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rs1064795764

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position92718999
GeneBICD2
is asnp
is mentioned by
dbSNPrs1064795764
dbSNP (old)rs1064795764
ClinGenrs1064795764
ebirs1064795764
HLIrs1064795764
Exacrs1064795764
Gnomadrs1064795764
Varsomers1064795764
Maprs1064795764
PheGenIrs1064795764
Biobankrs1064795764
1000 genomesrs1064795764
hgdprs1064795764
ensemblrs1064795764
gopubmedrs1064795764
geneviewrs1064795764
scholarrs1064795764
googlers1064795764
pharmgkbrs1064795764
gwascentralrs1064795764
openSNPrs1064795764
23andMers1064795764
23andMe allrs1064795764
SNPshotrs1064795764
SNPdbers1064795764
MSV3drs1064795764
GWAS Ctlgrs1064795764
Max Magnitude0
ClinVar
Risk rs1064795764(T;T)
Alt rs1064795764(T;T)
Reference Rs1064795764(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BICD2
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.95481281G>A
CLNSRC
CLNACC RCV000479919.1,