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rs1060502926

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502926(A;A)
Make rs1060502926(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47805028
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502926
dbSNP (old)rs1060502926
ClinGenrs1060502926
ebirs1060502926
HLIrs1060502926
Exacrs1060502926
Gnomadrs1060502926
Varsomers1060502926
Maprs1060502926
PheGenIrs1060502926
Biobankrs1060502926
1000 genomesrs1060502926
hgdprs1060502926
ensemblrs1060502926
gopubmedrs1060502926
geneviewrs1060502926
scholarrs1060502926
googlers1060502926
pharmgkbrs1060502926
gwascentralrs1060502926
openSNPrs1060502926
23andMers1060502926
23andMe allrs1060502926
SNPshotrs1060502926
SNPdbers1060502926
MSV3drs1060502926
GWAS Ctlgrs1060502926
Max Magnitude0
ClinVar
Risk rs1060502926(A;A)
Alt rs1060502926(A;A)
Reference Rs1060502926(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48032167G>A
CLNSRC
CLNACC RCV000475044.1,