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rs1064795653

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position47466717
GeneMSH2
is asnp
is mentioned by
dbSNPrs1064795653
dbSNP (old)rs1064795653
ClinGenrs1064795653
ebirs1064795653
HLIrs1064795653
Exacrs1064795653
Gnomadrs1064795653
Varsomers1064795653
Maprs1064795653
PheGenIrs1064795653
Biobankrs1064795653
1000 genomesrs1064795653
hgdprs1064795653
ensemblrs1064795653
gopubmedrs1064795653
geneviewrs1064795653
scholarrs1064795653
googlers1064795653
pharmgkbrs1064795653
gwascentralrs1064795653
openSNPrs1064795653
23andMers1064795653
23andMe allrs1064795653
SNPshotrs1064795653
SNPdbers1064795653
MSV3drs1064795653
GWAS Ctlgrs1064795653
Max Magnitude0
ClinVar
Risk rs1064795653(-;-)
Alt rs1064795653(-;-)
Reference Rs1064795653(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47693856delC
CLNSRC
CLNACC RCV000481233.1,