rs2013162
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2013162(A;A) |
Make rs2013162(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 209795339 |
Gene | IRF6 |
is a | snp |
is | mentioned by |
dbSNP | rs2013162 |
dbSNP (classic) | rs2013162 |
ClinGen | rs2013162 |
ebi | rs2013162 |
HLI | rs2013162 |
Exac | rs2013162 |
Gnomad | rs2013162 |
Varsome | rs2013162 |
LitVar | rs2013162 |
Map | rs2013162 |
PheGenI | rs2013162 |
Biobank | rs2013162 |
1000 genomes | rs2013162 |
hgdp | rs2013162 |
ensembl | rs2013162 |
geneview | rs2013162 |
scholar | rs2013162 |
rs2013162 | |
pharmgkb | rs2013162 |
gwascentral | rs2013162 |
openSNP | rs2013162 |
23andMe | rs2013162 |
SNPshot | rs2013162 |
SNPdbe | rs2013162 |
MSV3d | rs2013162 |
GWAS Ctlg | rs2013162 |
GMAF | 0.4031 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19734457] Association between IRF6 SNPs and oral clefts in West China
[PMID 15558496] Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population.
[PMID 17438386] Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations.
[PMID 18278815] Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway.
[PMID 18978678] Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.
[PMID 19521098] Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results.
[PMID 20403199] High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.
[PMID 23940636] TGFA and IRF6 Contribute to the Risk of Nonsyndromic Cleft Lip with or without Cleft Palate in Northeast China
ClinVar | |
---|---|
Risk | rs2013162(A;A) rs2013162(T;T) |
Alt | rs2013162(A;A) rs2013162(T;T) |
Reference | Rs2013162(C;C) |
Significance | Non-pathogenic |
Disease | not specified Popliteal pterygium syndrome Cleft Lip +/- Cleft Palate Van der Woude syndrome |
Variation | info |
Gene | IRF6 |
CLNDBN | not specified Popliteal pterygium syndrome Cleft Lip +/- Cleft Palate, Autosomal Dominant Van der Woude syndrome |
Reversed | 0 |
HGVS | NC_000001.10:g.209968684C>A |
CLNSRC | |
CLNACC | RCV000251393.1, RCV000288076.1, RCV000345570.1, RCV000402163.1, |