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rs1060502027

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502027(-;-)
Make rs1060502027(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47463049
GeneMSH2
is asnp
is mentioned by
dbSNPrs1060502027
dbSNP (old)rs1060502027
ClinGenrs1060502027
ebirs1060502027
HLIrs1060502027
Exacrs1060502027
Gnomadrs1060502027
Varsomers1060502027
Maprs1060502027
PheGenIrs1060502027
Biobankrs1060502027
1000 genomesrs1060502027
hgdprs1060502027
ensemblrs1060502027
gopubmedrs1060502027
geneviewrs1060502027
scholarrs1060502027
googlers1060502027
pharmgkbrs1060502027
gwascentralrs1060502027
openSNPrs1060502027
23andMers1060502027
23andMe allrs1060502027
SNPshotrs1060502027
SNPdbers1060502027
MSV3drs1060502027
GWAS Ctlgrs1060502027
Max Magnitude0
ClinVar
Risk rs1060502027(-;-)
Alt rs1060502027(-;-)
Reference Rs1060502027(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690188delC
CLNSRC
CLNACC RCV000470990.1,