rs481931
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs481931(A;A) |
Make rs481931(A;C) |
Make rs481931(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 94104460 |
Gene | ABCA4 |
is a | snp |
is | mentioned by |
dbSNP | rs481931 |
dbSNP (classic) | rs481931 |
ClinGen | rs481931 |
ebi | rs481931 |
HLI | rs481931 |
Exac | rs481931 |
Gnomad | rs481931 |
Varsome | rs481931 |
LitVar | rs481931 |
Map | rs481931 |
PheGenI | rs481931 |
Biobank | rs481931 |
1000 genomes | rs481931 |
hgdp | rs481931 |
ensembl | rs481931 |
geneview | rs481931 |
scholar | rs481931 |
rs481931 | |
pharmgkb | rs481931 |
gwascentral | rs481931 |
openSNP | rs481931 |
23andMe | rs481931 |
SNPshot | rs481931 |
SNPdbe | rs481931 |
MSV3d | rs481931 |
GWAS Ctlg | rs481931 |
Max Magnitude | 0 |
[PMID 25499508] A polymorphic marker associated with non-syndromic cleft lip with or without cleft palate in a population in Heilongjiang Province, northern China
[PMID 26586245] Polymorphic variants near 1p22 and 20q11.2 loci and the risk of non-syndromic cleft lip and palate in South Indian population