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rs1064792852

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position95247744
GeneC8orf37
is asnp
is mentioned by
dbSNPrs1064792852
dbSNP (old)rs1064792852
ClinGenrs1064792852
ebirs1064792852
HLIrs1064792852
Exacrs1064792852
Gnomadrs1064792852
Varsomers1064792852
Maprs1064792852
PheGenIrs1064792852
Biobankrs1064792852
1000 genomesrs1064792852
hgdprs1064792852
ensemblrs1064792852
gopubmedrs1064792852
geneviewrs1064792852
scholarrs1064792852
googlers1064792852
pharmgkbrs1064792852
gwascentralrs1064792852
openSNPrs1064792852
23andMers1064792852
23andMe allrs1064792852
SNPshotrs1064792852
SNPdbers1064792852
MSV3drs1064792852
GWAS Ctlgrs1064792852
Max Magnitude0
ClinVar
Risk rs1064792852(A;A)
Alt rs1064792852(A;A)
Reference Rs1064792852(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 64
Variation info
Gene C8orf37
CLNDBN Retinitis pigmentosa 64
Reversed 1
HGVS NC_000008.10:g.96259972A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024191.2,