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rs1060502946

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1060502946(-;AA)
Make rs1060502946(AA;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47799278
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502946
dbSNP (old)rs1060502946
ClinGenrs1060502946
ebirs1060502946
HLIrs1060502946
Exacrs1060502946
Gnomadrs1060502946
Varsomers1060502946
Maprs1060502946
PheGenIrs1060502946
Biobankrs1060502946
1000 genomesrs1060502946
hgdprs1060502946
ensemblrs1060502946
gopubmedrs1060502946
geneviewrs1060502946
scholarrs1060502946
googlers1060502946
pharmgkbrs1060502946
gwascentralrs1060502946
openSNPrs1060502946
23andMers1060502946
23andMe allrs1060502946
SNPshotrs1060502946
SNPdbers1060502946
MSV3drs1060502946
GWAS Ctlgrs1060502946
Max Magnitude0
ClinVar
Risk rs1060502946(AA;AA)
Alt rs1060502946(AA;AA)
Reference Rs1060502946(-;-)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026417_48026418insAA
CLNSRC
CLNACC RCV000462324.1,