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rs1064794071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTGACTT;TTGACTT) 0 common in clinvar
Chromosome2
Position47470969
GeneMSH2
is asnp
is mentioned by
dbSNPrs1064794071
dbSNP (old)rs1064794071
ClinGenrs1064794071
ebirs1064794071
HLIrs1064794071
Exacrs1064794071
Gnomadrs1064794071
Varsomers1064794071
LitVarrs1064794071
Maprs1064794071
PheGenIrs1064794071
Biobankrs1064794071
1000 genomesrs1064794071
hgdprs1064794071
ensemblrs1064794071
gopubmedrs1064794071
geneviewrs1064794071
scholarrs1064794071
googlers1064794071
pharmgkbrs1064794071
gwascentralrs1064794071
openSNPrs1064794071
23andMers1064794071
23andMe allrs1064794071
SNPshotrs1064794071
SNPdbers1064794071
MSV3drs1064794071
GWAS Ctlgrs1064794071
Max Magnitude0
ClinVar
Risk rs1064794071(-;-)
Alt rs1064794071(-;-)
Reference Rs1064794071(TTGACTT;TTGACTT)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47698108_47698114delTTGACTT
CLNSRC
CLNACC RCV000484239.1,