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rs387907137

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907137(A;G)
Make rs387907137(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position95247696
GeneC8orf37
is asnp
is mentioned by
dbSNPrs387907137
ebirs387907137
HLIrs387907137
Exacrs387907137
Varsomers387907137
Maprs387907137
PheGenIrs387907137
hapmaprs387907137
1000 genomesrs387907137
hgdprs387907137
ensemblrs387907137
gopubmedrs387907137
geneviewrs387907137
scholarrs387907137
googlers387907137
pharmgkbrs387907137
gwascentralrs387907137
openSNPrs387907137
23andMers387907137
23andMe allrs387907137
SNP Nexus

SNPshotrs387907137
SNPdbers387907137
MSV3drs387907137
GWAS Ctlgrs387907137
Max Magnitude0
ClinVar
Risk rs387907137(G;G)
Alt rs387907137(G;G)
Reference rs387907137(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 64
Variation info
Gene C8orf37
CLNDBN Retinitis pigmentosa 64
Reversed 1
HGVS NC_000008.10:g.96259924T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000024194.2,