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rs1060502890

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502890(-;-)
Make rs1060502890(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47800974
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502890
dbSNP (old)rs1060502890
ClinGenrs1060502890
ebirs1060502890
HLIrs1060502890
Exacrs1060502890
Gnomadrs1060502890
Varsomers1060502890
Maprs1060502890
PheGenIrs1060502890
Biobankrs1060502890
1000 genomesrs1060502890
hgdprs1060502890
ensemblrs1060502890
gopubmedrs1060502890
geneviewrs1060502890
scholarrs1060502890
googlers1060502890
pharmgkbrs1060502890
gwascentralrs1060502890
openSNPrs1060502890
23andMers1060502890
23andMe allrs1060502890
SNPshotrs1060502890
SNPdbers1060502890
MSV3drs1060502890
GWAS Ctlgrs1060502890
Max Magnitude0
ClinVar
Risk rs1060502890(-;-)
Alt rs1060502890(-;-)
Reference Rs1060502890(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028113delA
CLNSRC
CLNACC RCV000472587.1,