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rs1064793561

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTAC;TTAC) 0 common in clinvar
Chromosome2
Position47466712
GeneMSH2
is asnp
is mentioned by
dbSNPrs1064793561
dbSNP (classic)rs1064793561
ClinGenrs1064793561
ebirs1064793561
HLIrs1064793561
Exacrs1064793561
Gnomadrs1064793561
Varsomers1064793561
LitVarrs1064793561
Maprs1064793561
PheGenIrs1064793561
Biobankrs1064793561
1000 genomesrs1064793561
hgdprs1064793561
ensemblrs1064793561
geneviewrs1064793561
scholarrs1064793561
googlers1064793561
pharmgkbrs1064793561
gwascentralrs1064793561
openSNPrs1064793561
23andMers1064793561
23andMe allrs1064793561
SNPshotrs1064793561
SNPdbers1064793561
MSV3drs1064793561
GWAS Ctlgrs1064793561
Max Magnitude0
ClinVar
Risk rs1064793561(-;-)
Alt rs1064793561(-;-)
Reference Rs1064793561(TTAC;TTAC)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47693851_47693854delACTT
CLNSRC
CLNACC RCV000485928.1,