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rs750528093

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs750528093(G;G)
Make rs750528093(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799278
GeneMSH6
is asnp
is mentioned by
dbSNPrs750528093
ebirs750528093
HLIrs750528093
Exacrs750528093
Varsomers750528093
Maprs750528093
PheGenIrs750528093
hapmaprs750528093
1000 genomesrs750528093
hgdprs750528093
ensemblrs750528093
gopubmedrs750528093
geneviewrs750528093
scholarrs750528093
googlers750528093
pharmgkbrs750528093
gwascentralrs750528093
openSNPrs750528093
23andMers750528093
23andMe allrs750528093
SNP Nexus

SNPshotrs750528093
SNPdbers750528093
MSV3drs750528093
GWAS Ctlgrs750528093
Max Magnitude0
ClinVar
Risk rs750528093(C,G;C,G)
Alt rs750528093(C,G;C,G)
Reference rs750528093(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026417T>C
CLNSRC
CLNACC RCV000162486.1,