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rs761033647

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761033647(C;T)
Make rs761033647(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47783408
GeneMSH6
is asnp
is mentioned by
dbSNPrs761033647
ebirs761033647
HLIrs761033647
Exacrs761033647
Varsomers761033647
Maprs761033647
PheGenIrs761033647
hapmaprs761033647
1000 genomesrs761033647
hgdprs761033647
ensemblrs761033647
gopubmedrs761033647
geneviewrs761033647
scholarrs761033647
googlers761033647
pharmgkbrs761033647
gwascentralrs761033647
openSNPrs761033647
23andMers761033647
23andMe allrs761033647
SNP Nexus

SNPshotrs761033647
SNPdbers761033647
MSV3drs761033647
GWAS Ctlgrs761033647
Max Magnitude0
ClinVar
Risk rs761033647(T;T)
Alt rs761033647(T;T)
Reference rs761033647(C;C)
Significance Probable-Pathogenic
Disease Hereditary nonpolyposis colorectal cancer type 5
Variation info
Gene MSH6
CLNDBN Hereditary nonpolyposis colorectal cancer type 5
Reversed 0
HGVS NC_000002.11:g.48010547C>A
CLNSRC
CLNACC RCV000184046.2,