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rs1060502029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAAG;GAAG) 0 common in clinvar
Make rs1060502029(AAA;AAA)
Make rs1060502029(AAA;GAAG)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47463114
GeneMSH2
is asnp
is mentioned by
dbSNPrs1060502029
dbSNP (old)rs1060502029
ClinGenrs1060502029
ebirs1060502029
HLIrs1060502029
Exacrs1060502029
Gnomadrs1060502029
Varsomers1060502029
Maprs1060502029
PheGenIrs1060502029
Biobankrs1060502029
1000 genomesrs1060502029
hgdprs1060502029
ensemblrs1060502029
gopubmedrs1060502029
geneviewrs1060502029
scholarrs1060502029
googlers1060502029
pharmgkbrs1060502029
gwascentralrs1060502029
openSNPrs1060502029
23andMers1060502029
23andMe allrs1060502029
SNPshotrs1060502029
SNPdbers1060502029
MSV3drs1060502029
GWAS Ctlgrs1060502029
Max Magnitude0
ClinVar
Risk rs1060502029(AAA;AAA)
Alt rs1060502029(AAA;AAA)
Reference Rs1060502029(GAAG;GAAG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690253_47690256delGAAGinsAAA
CLNSRC
CLNACC RCV000470495.1,