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rs1064794943

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position47800972
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064794943
dbSNP (old)rs1064794943
ClinGenrs1064794943
ebirs1064794943
HLIrs1064794943
Exacrs1064794943
Gnomadrs1064794943
Varsomers1064794943
Maprs1064794943
PheGenIrs1064794943
Biobankrs1064794943
1000 genomesrs1064794943
hgdprs1064794943
ensemblrs1064794943
gopubmedrs1064794943
geneviewrs1064794943
scholarrs1064794943
googlers1064794943
pharmgkbrs1064794943
gwascentralrs1064794943
openSNPrs1064794943
23andMers1064794943
23andMe allrs1064794943
SNPshotrs1064794943
SNPdbers1064794943
MSV3drs1064794943
GWAS Ctlgrs1064794943
Max Magnitude0
ClinVar
Risk rs1064794943(T;T)
Alt rs1064794943(T;T)
Reference Rs1064794943(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48028111A>T
CLNSRC
CLNACC RCV000478571.1,