rs2224391
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs2224391(A;C) |
Make rs2224391(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 5260703 |
Gene | FARS2, LYRM4 |
is a | snp |
is | mentioned by |
dbSNP | rs2224391 |
dbSNP (classic) | rs2224391 |
ClinGen | rs2224391 |
ebi | rs2224391 |
HLI | rs2224391 |
Exac | rs2224391 |
Gnomad | rs2224391 |
Varsome | rs2224391 |
LitVar | rs2224391 |
Map | rs2224391 |
PheGenI | rs2224391 |
Biobank | rs2224391 |
1000 genomes | rs2224391 |
hgdp | rs2224391 |
ensembl | rs2224391 |
geneview | rs2224391 |
scholar | rs2224391 |
rs2224391 | |
pharmgkb | rs2224391 |
gwascentral | rs2224391 |
openSNP | rs2224391 |
23andMe | rs2224391 |
SNPshot | rs2224391 |
SNPdbe | rs2224391 |
MSV3d | rs2224391 |
GWAS Ctlg | rs2224391 |
GMAF | 0.3926 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21998595] |
Trait | |
Title | Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry. |
Risk Allele | A |
P-val | 0.000003 |
Odds Ratio | 0.0490 None |
[PMID 21968932] Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.
ClinVar | |
---|---|
Risk | rs2224391(C;C) |
Alt | rs2224391(C;C) |
Reference | Rs2224391(A;A) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | FARS2 LYRM4 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000006.11:g.5260936A>C |
CLNSRC | |
CLNACC | RCV000443713.1, |