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rs1064795127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position47475148
GeneMSH2
is asnp
is mentioned by
dbSNPrs1064795127
dbSNP (classic)rs1064795127
ClinGenrs1064795127
ebirs1064795127
HLIrs1064795127
Exacrs1064795127
Gnomadrs1064795127
Varsomers1064795127
LitVarrs1064795127
Maprs1064795127
PheGenIrs1064795127
Biobankrs1064795127
1000 genomesrs1064795127
hgdprs1064795127
ensemblrs1064795127
geneviewrs1064795127
scholarrs1064795127
googlers1064795127
pharmgkbrs1064795127
gwascentralrs1064795127
openSNPrs1064795127
23andMers1064795127
23andMe allrs1064795127
SNPshotrs1064795127
SNPdbers1064795127
MSV3drs1064795127
GWAS Ctlgrs1064795127
Max Magnitude0
ClinVar
Risk rs1064795127(-;-)
Alt rs1064795127(-;-)
Reference Rs1064795127(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47702287delG
CLNSRC
CLNACC RCV000482381.1,