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rs121912631

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912631(A;A)
Make rs121912631(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position71811530
GeneNR2E3
is asnp
is mentioned by
dbSNPrs121912631
ebirs121912631
HLIrs121912631
Exacrs121912631
Varsomers121912631
Maprs121912631
PheGenIrs121912631
hapmaprs121912631
1000 genomesrs121912631
hgdprs121912631
ensemblrs121912631
gopubmedrs121912631
geneviewrs121912631
scholarrs121912631
googlers121912631
pharmgkbrs121912631
gwascentralrs121912631
openSNPrs121912631
23andMers121912631
23andMe allrs121912631
SNP Nexus

SNPshotrs121912631
SNPdbers121912631
MSV3drs121912631
GWAS Ctlgrs121912631
Max Magnitude0
OMIM604485
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121912631(A,T;A,T)
Alt rs121912631(A,T;A,T)
Reference rs121912631(G;G)
Significance Other
Disease Retinitis pigmentosa 37
Variation info
Gene NR2E3
CLNDBN Retinitis pigmentosa 37
Reversed 0
HGVS NC_000015.9:g.72103870G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005871.3,