Have questions? Visit https://www.reddit.com/r/SNPedia

rs372929441

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372929441(A;A)
Make rs372929441(A;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position84022883
GeneSLC38A8
is asnp
is mentioned by
dbSNPrs372929441
ebirs372929441
HLIrs372929441
Exacrs372929441
Varsomers372929441
Maprs372929441
PheGenIrs372929441
hapmaprs372929441
1000 genomesrs372929441
hgdprs372929441
ensemblrs372929441
gopubmedrs372929441
geneviewrs372929441
scholarrs372929441
googlers372929441
pharmgkbrs372929441
gwascentralrs372929441
openSNPrs372929441
23andMers372929441
23andMe allrs372929441
SNP Nexus

SNPshotrs372929441
SNPdbers372929441
MSV3drs372929441
GWAS Ctlgrs372929441
Max Magnitude0
ClinVar
Risk rs372929441(A,T;A,T)
Alt rs372929441(A,T;A,T)
Reference rs372929441(C;C)
Significance Pathogenic
Disease Foveal hypoplasia 2
Variation info
Gene SLC38A8
CLNDBN Foveal hypoplasia 2
Reversed 0
HGVS NC_000016.9:g.84056488C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000111471.3,