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rs121434551

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434551(A;A)
Make rs121434551(A;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position60158357
GeneCA4
is asnp
is mentioned by
dbSNPrs121434551
ebirs121434551
HLIrs121434551
Exacrs121434551
Varsomers121434551
Maprs121434551
PheGenIrs121434551
hapmaprs121434551
1000 genomesrs121434551
hgdprs121434551
ensemblrs121434551
gopubmedrs121434551
geneviewrs121434551
scholarrs121434551
googlers121434551
pharmgkbrs121434551
gwascentralrs121434551
openSNPrs121434551
23andMers121434551
23andMe allrs121434551
SNP Nexus

SNPshotrs121434551
SNPdbers121434551
MSV3drs121434551
GWAS Ctlgrs121434551
Max Magnitude0
OMIM114760
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434551(A,T;A,T)
Alt rs121434551(A,T;A,T)
Reference rs121434551(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 17
Variation info
Gene CA4
CLNDBN Retinitis pigmentosa 17
Reversed 0
HGVS NC_000017.10:g.58235718C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019174.28,