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rs587777272

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777272(A;C)
Make rs587777272(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position170467249
GeneSLC7A14
is asnp
is mentioned by
dbSNPrs587777272
ebirs587777272
HLIrs587777272
Exacrs587777272
Varsomers587777272
Maprs587777272
PheGenIrs587777272
hapmaprs587777272
1000 genomesrs587777272
hgdprs587777272
ensemblrs587777272
gopubmedrs587777272
geneviewrs587777272
scholarrs587777272
googlers587777272
pharmgkbrs587777272
gwascentralrs587777272
openSNPrs587777272
23andMers587777272
23andMe allrs587777272
SNP Nexus

SNPshotrs587777272
SNPdbers587777272
MSV3drs587777272
GWAS Ctlgrs587777272
Max Magnitude0
ClinVar
Risk rs587777272(A,C;A,C)
Alt rs587777272(A,C;A,C)
Reference rs587777272(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 68
Variation info
Gene SLC7A14
CLNDBN Retinitis pigmentosa 68
Reversed 1
HGVS NC_000003.11:g.170185037A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000114375.2,