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rs387907136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907136(C;T)
Make rs387907136(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position95247712
GeneC8orf37
is asnp
is mentioned by
dbSNPrs387907136
ebirs387907136
HLIrs387907136
Exacrs387907136
Varsomers387907136
Maprs387907136
PheGenIrs387907136
hapmaprs387907136
1000 genomesrs387907136
hgdprs387907136
ensemblrs387907136
gopubmedrs387907136
geneviewrs387907136
scholarrs387907136
googlers387907136
pharmgkbrs387907136
gwascentralrs387907136
openSNPrs387907136
23andMers387907136
23andMe allrs387907136
SNP Nexus

SNPshotrs387907136
SNPdbers387907136
MSV3drs387907136
GWAS Ctlgrs387907136
Max Magnitude0
ClinVar
Risk rs387907136(T;T)
Alt rs387907136(T;T)
Reference rs387907136(C;C)
Significance Pathogenic
Disease Cone-rod dystrophy 16
Variation info
Gene C8orf37
CLNDBN Cone-rod dystrophy 16
Reversed 1
HGVS NC_000008.10:g.96259940G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024193.2,