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rs1060502882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502882(-;-)
Make rs1060502882(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47801132
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502882
dbSNP (old)rs1060502882
ClinGenrs1060502882
ebirs1060502882
HLIrs1060502882
Exacrs1060502882
Gnomadrs1060502882
Varsomers1060502882
Maprs1060502882
PheGenIrs1060502882
Biobankrs1060502882
1000 genomesrs1060502882
hgdprs1060502882
ensemblrs1060502882
gopubmedrs1060502882
geneviewrs1060502882
scholarrs1060502882
googlers1060502882
pharmgkbrs1060502882
gwascentralrs1060502882
openSNPrs1060502882
23andMers1060502882
23andMe allrs1060502882
SNPshotrs1060502882
SNPdbers1060502882
MSV3drs1060502882
GWAS Ctlgrs1060502882
Max Magnitude0
ClinVar
Risk rs1060502882(-;-)
Alt rs1060502882(-;-)
Reference Rs1060502882(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028271delC
CLNSRC
CLNACC RCV000473512.1,