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rs1064795960

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position47800105
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064795960
dbSNP (old)rs1064795960
ClinGenrs1064795960
ebirs1064795960
HLIrs1064795960
Exacrs1064795960
Gnomadrs1064795960
Varsomers1064795960
Maprs1064795960
PheGenIrs1064795960
Biobankrs1064795960
1000 genomesrs1064795960
hgdprs1064795960
ensemblrs1064795960
gopubmedrs1064795960
geneviewrs1064795960
scholarrs1064795960
googlers1064795960
pharmgkbrs1064795960
gwascentralrs1064795960
openSNPrs1064795960
23andMers1064795960
23andMe allrs1064795960
SNPshotrs1064795960
SNPdbers1064795960
MSV3drs1064795960
GWAS Ctlgrs1064795960
Max Magnitude0
ClinVar
Risk rs1064795960(T;T)
Alt rs1064795960(T;T)
Reference Rs1064795960(G;G)
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.48027244G>T
CLNSRC
CLNACC RCV000486081.1, RCV000491313.1,