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rs2013162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2013162(A;A)
Make rs2013162(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position209795339
GeneIRF6
is asnp
is mentioned by
dbSNPrs2013162
dbSNP (classic)rs2013162
ClinGenrs2013162
ebirs2013162
HLIrs2013162
Exacrs2013162
Gnomadrs2013162
Varsomers2013162
LitVarrs2013162
Maprs2013162
PheGenIrs2013162
Biobankrs2013162
1000 genomesrs2013162
hgdprs2013162
ensemblrs2013162
geneviewrs2013162
scholarrs2013162
googlers2013162
pharmgkbrs2013162
gwascentralrs2013162
openSNPrs2013162
23andMers2013162
SNPshotrs2013162
SNPdbers2013162
MSV3drs2013162
GWAS Ctlgrs2013162
GMAF0.4031
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 19734457OA-icon.png] Association between IRF6 SNPs and oral clefts in West China


[PMID 15558496OA-icon.png] 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 17438386OA-icon.png] Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations.


[PMID 18278815OA-icon.png] 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 18978678OA-icon.png] Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.


[PMID 19521098OA-icon.png] 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 20403199OA-icon.png] High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.


[PMID 23940636OA-icon.png] 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,