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rs1060502891

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502891(-;-)
Make rs1060502891(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47803500
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502891
dbSNP (old)rs1060502891
ClinGenrs1060502891
ebirs1060502891
HLIrs1060502891
Exacrs1060502891
Gnomadrs1060502891
Varsomers1060502891
Maprs1060502891
PheGenIrs1060502891
Biobankrs1060502891
1000 genomesrs1060502891
hgdprs1060502891
ensemblrs1060502891
gopubmedrs1060502891
geneviewrs1060502891
scholarrs1060502891
googlers1060502891
pharmgkbrs1060502891
gwascentralrs1060502891
openSNPrs1060502891
23andMers1060502891
23andMe allrs1060502891
SNPshotrs1060502891
SNPdbers1060502891
MSV3drs1060502891
GWAS Ctlgrs1060502891
Max Magnitude0
ClinVar
Risk rs1060502891(-;-)
Alt rs1060502891(-;-)
Reference Rs1060502891(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030639delA
CLNSRC
CLNACC RCV000460971.1,