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rs1064794755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome22
Position46343317
GeneTRMU
is asnp
is mentioned by
dbSNPrs1064794755
dbSNP (old)rs1064794755
ClinGenrs1064794755
ebirs1064794755
HLIrs1064794755
Exacrs1064794755
Gnomadrs1064794755
Varsomers1064794755
LitVarrs1064794755
Maprs1064794755
PheGenIrs1064794755
Biobankrs1064794755
1000 genomesrs1064794755
hgdprs1064794755
ensemblrs1064794755
gopubmedrs1064794755
geneviewrs1064794755
scholarrs1064794755
googlers1064794755
pharmgkbrs1064794755
gwascentralrs1064794755
openSNPrs1064794755
23andMers1064794755
23andMe allrs1064794755
SNPshotrs1064794755
SNPdbers1064794755
MSV3drs1064794755
GWAS Ctlgrs1064794755
Max Magnitude0
ClinVar
Risk rs1064794755(G;G)
Alt rs1064794755(G;G)
Reference Rs1064794755(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRMU
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.46739214A>G
CLNSRC
CLNACC RCV000482789.1,