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rs1064795843

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position93809101
GeneTMEM67
is asnp
is mentioned by
dbSNPrs1064795843
dbSNP (classic)rs1064795843
ClinGenrs1064795843
ebirs1064795843
HLIrs1064795843
Exacrs1064795843
Gnomadrs1064795843
Varsomers1064795843
LitVarrs1064795843
Maprs1064795843
PheGenIrs1064795843
Biobankrs1064795843
1000 genomesrs1064795843
hgdprs1064795843
ensemblrs1064795843
geneviewrs1064795843
scholarrs1064795843
googlers1064795843
pharmgkbrs1064795843
gwascentralrs1064795843
openSNPrs1064795843
23andMers1064795843
SNPshotrs1064795843
SNPdbers1064795843
MSV3drs1064795843
GWAS Ctlgrs1064795843
Max Magnitude0
ClinVar
Risk rs1064795843(-;-)
Alt rs1064795843(-;-)
Reference Rs1064795843(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TMEM67
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.94821329delT
CLNSRC
CLNACC RCV000480379.1,