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rs1064794075

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Chromosome2
Position47783495
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064794075
dbSNP (old)rs1064794075
ClinGenrs1064794075
ebirs1064794075
HLIrs1064794075
Exacrs1064794075
Gnomadrs1064794075
Varsomers1064794075
Maprs1064794075
PheGenIrs1064794075
Biobankrs1064794075
1000 genomesrs1064794075
hgdprs1064794075
ensemblrs1064794075
gopubmedrs1064794075
geneviewrs1064794075
scholarrs1064794075
googlers1064794075
pharmgkbrs1064794075
gwascentralrs1064794075
openSNPrs1064794075
23andMers1064794075
23andMe allrs1064794075
SNPshotrs1064794075
SNPdbers1064794075
MSV3drs1064794075
GWAS Ctlgrs1064794075
Max Magnitude0
ClinVar
Risk rs1064794075(AG;AG)
Alt rs1064794075(AG;AG)
Reference Rs1064794075(TA;TA)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48010634_48010635delTAinsAG
CLNSRC
CLNACC RCV000479300.1, RCV000491081.1,