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rs786201042

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201042(C;T)
Make rs786201042(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47783243
GeneMSH6
is asnp
is mentioned by
dbSNPrs786201042
ebirs786201042
HLIrs786201042
Exacrs786201042
Varsomers786201042
Maprs786201042
PheGenIrs786201042
hapmaprs786201042
1000 genomesrs786201042
hgdprs786201042
ensemblrs786201042
gopubmedrs786201042
geneviewrs786201042
scholarrs786201042
googlers786201042
pharmgkbrs786201042
gwascentralrs786201042
openSNPrs786201042
23andMers786201042
23andMe allrs786201042
SNP Nexus

SNPshotrs786201042
SNPdbers786201042
MSV3drs786201042
GWAS Ctlgrs786201042
Max Magnitude0
ClinVar
Risk rs786201042(T;T)
Alt rs786201042(T;T)
Reference rs786201042(C;C)
Significance Other
Disease Hereditary cancer-predisposing syndrome Lynch syndrome not provided Hereditary nonpolyposis colorectal cancer type 5
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome not provided Hereditary nonpolyposis colorectal cancer type 5
Reversed 0
HGVS NC_000002.11:g.48010382C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000162425.1, RCV000199142.4, RCV000202232.2, RCV000202528.1,