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rs1064794164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Chromosome2
Position47800483
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064794164
dbSNP (old)rs1064794164
ClinGenrs1064794164
ebirs1064794164
HLIrs1064794164
Exacrs1064794164
Gnomadrs1064794164
Varsomers1064794164
LitVarrs1064794164
Maprs1064794164
PheGenIrs1064794164
Biobankrs1064794164
1000 genomesrs1064794164
hgdprs1064794164
ensemblrs1064794164
gopubmedrs1064794164
geneviewrs1064794164
scholarrs1064794164
googlers1064794164
pharmgkbrs1064794164
gwascentralrs1064794164
openSNPrs1064794164
23andMers1064794164
23andMe allrs1064794164
SNPshotrs1064794164
SNPdbers1064794164
MSV3drs1064794164
GWAS Ctlgrs1064794164
Max Magnitude0
ClinVar
Risk rs1064794164(-;-)
Alt rs1064794164(-;-)
Reference Rs1064794164(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48027622_48027623delAG
CLNSRC
CLNACC RCV000487254.1,