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rs1064796988

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome12
Position80355885
GeneOTOGL
is asnp
is mentioned by
dbSNPrs1064796988
dbSNP (classic)rs1064796988
ClinGenrs1064796988
ebirs1064796988
HLIrs1064796988
Exacrs1064796988
Gnomadrs1064796988
Varsomers1064796988
LitVarrs1064796988
Maprs1064796988
PheGenIrs1064796988
Biobankrs1064796988
1000 genomesrs1064796988
hgdprs1064796988
ensemblrs1064796988
geneviewrs1064796988
scholarrs1064796988
googlers1064796988
pharmgkbrs1064796988
gwascentralrs1064796988
openSNPrs1064796988
23andMers1064796988
23andMe allrs1064796988
SNPshotrs1064796988
SNPdbers1064796988
MSV3drs1064796988
GWAS Ctlgrs1064796988
Max Magnitude0
ClinVar
Risk rs1064796988(T;T)
Alt rs1064796988(T;T)
Reference Rs1064796988(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OTOGL
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.80749665C>T
CLNSRC
CLNACC RCV000479777.1,