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rs1064794028

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Chromosome2
Position47799981
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064794028
dbSNP (old)rs1064794028
ClinGenrs1064794028
ebirs1064794028
HLIrs1064794028
Exacrs1064794028
Gnomadrs1064794028
Varsomers1064794028
Maprs1064794028
PheGenIrs1064794028
Biobankrs1064794028
1000 genomesrs1064794028
hgdprs1064794028
ensemblrs1064794028
gopubmedrs1064794028
geneviewrs1064794028
scholarrs1064794028
googlers1064794028
pharmgkbrs1064794028
gwascentralrs1064794028
openSNPrs1064794028
23andMers1064794028
23andMe allrs1064794028
SNPshotrs1064794028
SNPdbers1064794028
MSV3drs1064794028
GWAS Ctlgrs1064794028
Max Magnitude0
ClinVar
Risk rs1064794028(-;-)
Alt rs1064794028(-;-)
Reference Rs1064794028(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48027120_48027121delTG
CLNSRC
CLNACC RCV000481527.1,