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rs1064794388

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Chromosome2
Position47799579
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064794388
dbSNP (old)rs1064794388
ClinGenrs1064794388
ebirs1064794388
HLIrs1064794388
Exacrs1064794388
Gnomadrs1064794388
Varsomers1064794388
Maprs1064794388
PheGenIrs1064794388
Biobankrs1064794388
1000 genomesrs1064794388
hgdprs1064794388
ensemblrs1064794388
gopubmedrs1064794388
geneviewrs1064794388
scholarrs1064794388
googlers1064794388
pharmgkbrs1064794388
gwascentralrs1064794388
openSNPrs1064794388
23andMers1064794388
23andMe allrs1064794388
SNPshotrs1064794388
SNPdbers1064794388
MSV3drs1064794388
GWAS Ctlgrs1064794388
Max Magnitude0
ClinVar
Risk rs1064794388(-;-)
Alt rs1064794388(-;-)
Reference Rs1064794388(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48026718_48026719delTG
CLNSRC
CLNACC RCV000480986.1,