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rs1064792853

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome8
Position95263776
GeneC8orf37
is asnp
is mentioned by
dbSNPrs1064792853
dbSNP (old)rs1064792853
ClinGenrs1064792853
ebirs1064792853
HLIrs1064792853
Exacrs1064792853
Gnomadrs1064792853
Varsomers1064792853
Maprs1064792853
PheGenIrs1064792853
Biobankrs1064792853
1000 genomesrs1064792853
hgdprs1064792853
ensemblrs1064792853
gopubmedrs1064792853
geneviewrs1064792853
scholarrs1064792853
googlers1064792853
pharmgkbrs1064792853
gwascentralrs1064792853
openSNPrs1064792853
23andMers1064792853
23andMe allrs1064792853
SNPshotrs1064792853
SNPdbers1064792853
MSV3drs1064792853
GWAS Ctlgrs1064792853
Max Magnitude0
ClinVar
Risk rs1064792853(G;G)
Alt rs1064792853(G;G)
Reference Rs1064792853(A;A)
Significance Pathogenic
Disease Cone-rod dystrophy 16
Variation info
Gene C8orf37
CLNDBN Cone-rod dystrophy 16
Reversed 1
HGVS NC_000008.10:g.96276004T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000024192.3,