Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060502876

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502876(A;A)
Make rs1060502876(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47800718
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502876
dbSNP (old)rs1060502876
ClinGenrs1060502876
ebirs1060502876
HLIrs1060502876
Exacrs1060502876
Gnomadrs1060502876
Varsomers1060502876
Maprs1060502876
PheGenIrs1060502876
Biobankrs1060502876
1000 genomesrs1060502876
hgdprs1060502876
ensemblrs1060502876
gopubmedrs1060502876
geneviewrs1060502876
scholarrs1060502876
googlers1060502876
pharmgkbrs1060502876
gwascentralrs1060502876
openSNPrs1060502876
23andMers1060502876
23andMe allrs1060502876
SNPshotrs1060502876
SNPdbers1060502876
MSV3drs1060502876
GWAS Ctlgrs1060502876
Max Magnitude0
ClinVar
Risk rs1060502876(A;A)
Alt rs1060502876(A;A)
Reference Rs1060502876(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027857G>A
CLNSRC
CLNACC RCV000470184.1,