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

rs587777273

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777273(A;A)
Make rs587777273(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position170501255
GeneSLC7A14
is asnp
is mentioned by
dbSNPrs587777273
ebirs587777273
HLIrs587777273
Exacrs587777273
Varsomers587777273
Maprs587777273
PheGenIrs587777273
hapmaprs587777273
1000 genomesrs587777273
hgdprs587777273
ensemblrs587777273
gopubmedrs587777273
geneviewrs587777273
scholarrs587777273
googlers587777273
pharmgkbrs587777273
gwascentralrs587777273
openSNPrs587777273
23andMers587777273
23andMe allrs587777273
SNP Nexus

SNPshotrs587777273
SNPdbers587777273
MSV3drs587777273
GWAS Ctlgrs587777273
Max Magnitude0
ClinVar
Risk rs587777273(A,G;A,G)
Alt rs587777273(A,G;A,G)
Reference rs587777273(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 68
Variation info
Gene SLC7A14
CLNDBN Retinitis pigmentosa 68
Reversed 1
HGVS NC_000003.11:g.170219044G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114377.2,