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rs1060502901

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502901(G;G)
Make rs1060502901(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47803435
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502901
dbSNP (old)rs1060502901
ClinGenrs1060502901
ebirs1060502901
HLIrs1060502901
Exacrs1060502901
Gnomadrs1060502901
Varsomers1060502901
Maprs1060502901
PheGenIrs1060502901
Biobankrs1060502901
1000 genomesrs1060502901
hgdprs1060502901
ensemblrs1060502901
gopubmedrs1060502901
geneviewrs1060502901
scholarrs1060502901
googlers1060502901
pharmgkbrs1060502901
gwascentralrs1060502901
openSNPrs1060502901
23andMers1060502901
23andMe allrs1060502901
SNPshotrs1060502901
SNPdbers1060502901
MSV3drs1060502901
GWAS Ctlgrs1060502901
Max Magnitude0
ClinVar
Risk rs1060502901(G;G)
Alt rs1060502901(G;G)
Reference Rs1060502901(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48030574T>G
CLNSRC
CLNACC RCV000468032.1, RCV000491375.1,