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rs1064794155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position47412561
GeneMSH2
is asnp
is mentioned by
dbSNPrs1064794155
dbSNP (old)rs1064794155
ClinGenrs1064794155
ebirs1064794155
HLIrs1064794155
Exacrs1064794155
Gnomadrs1064794155
Varsomers1064794155
Maprs1064794155
PheGenIrs1064794155
Biobankrs1064794155
1000 genomesrs1064794155
hgdprs1064794155
ensemblrs1064794155
gopubmedrs1064794155
geneviewrs1064794155
scholarrs1064794155
googlers1064794155
pharmgkbrs1064794155
gwascentralrs1064794155
openSNPrs1064794155
23andMers1064794155
23andMe allrs1064794155
SNPshotrs1064794155
SNPdbers1064794155
MSV3drs1064794155
GWAS Ctlgrs1064794155
Max Magnitude0
ClinVar
Risk rs1064794155(-;-)
Alt rs1064794155(-;-)
Reference Rs1064794155(G;G)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47639700delG
CLNSRC
CLNACC RCV000485573.1, RCV000491720.1,