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rs1060502941

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502941(-;-)
Make rs1060502941(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47798879
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502941
dbSNP (old)rs1060502941
ClinGenrs1060502941
ebirs1060502941
HLIrs1060502941
Exacrs1060502941
Gnomadrs1060502941
Varsomers1060502941
Maprs1060502941
PheGenIrs1060502941
Biobankrs1060502941
1000 genomesrs1060502941
hgdprs1060502941
ensemblrs1060502941
gopubmedrs1060502941
geneviewrs1060502941
scholarrs1060502941
googlers1060502941
pharmgkbrs1060502941
gwascentralrs1060502941
openSNPrs1060502941
23andMers1060502941
23andMe allrs1060502941
SNPshotrs1060502941
SNPdbers1060502941
MSV3drs1060502941
GWAS Ctlgrs1060502941
Max Magnitude0
ClinVar
Risk rs1060502941(-;-)
Alt rs1060502941(-;-)
Reference Rs1060502941(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026018delA
CLNSRC
CLNACC RCV000466552.1,