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rs1060502932

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502932(-;-)
Make rs1060502932(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47798982
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502932
dbSNP (old)rs1060502932
ClinGenrs1060502932
ebirs1060502932
HLIrs1060502932
Exacrs1060502932
Gnomadrs1060502932
Varsomers1060502932
Maprs1060502932
PheGenIrs1060502932
Biobankrs1060502932
1000 genomesrs1060502932
hgdprs1060502932
ensemblrs1060502932
gopubmedrs1060502932
geneviewrs1060502932
scholarrs1060502932
googlers1060502932
pharmgkbrs1060502932
gwascentralrs1060502932
openSNPrs1060502932
23andMers1060502932
23andMe allrs1060502932
SNPshotrs1060502932
SNPdbers1060502932
MSV3drs1060502932
GWAS Ctlgrs1060502932
Max Magnitude0
ClinVar
Risk rs1060502932(-;-)
Alt rs1060502932(-;-)
Reference Rs1060502932(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026121delC
CLNSRC
CLNACC RCV000456722.1,