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rs1085307121

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position95269033
GeneC8orf37, C8orf37-AS1
is asnp
is mentioned by
dbSNPrs1085307121
dbSNP (old)rs1085307121
ClinGenrs1085307121
ebirs1085307121
HLIrs1085307121
Exacrs1085307121
Gnomadrs1085307121
Varsomers1085307121
Maprs1085307121
PheGenIrs1085307121
Biobankrs1085307121
1000 genomesrs1085307121
hgdprs1085307121
ensemblrs1085307121
gopubmedrs1085307121
geneviewrs1085307121
scholarrs1085307121
googlers1085307121
pharmgkbrs1085307121
gwascentralrs1085307121
openSNPrs1085307121
23andMers1085307121
23andMe allrs1085307121
SNPshotrs1085307121
SNPdbers1085307121
MSV3drs1085307121
GWAS Ctlgrs1085307121
Max Magnitude0
ClinVar
Risk rs1085307121(C;C)
Alt rs1085307121(C;C)
Reference Rs1085307121(T;T)
Significance Pathogenic
Disease Cone-rod dystrophy 16
Variation info
Gene C8orf37-AS1 C8orf37
CLNDBN Cone-rod dystrophy 16
Reversed 1
HGVS NC_000008.10:g.96281261A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000477722.1,