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rs63751407

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs63751407(-;-)
Make rs63751407(-;CT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47801035
GeneMSH6
is asnp
is mentioned by
dbSNPrs63751407
ebirs63751407
HLIrs63751407
Exacrs63751407
Varsomers63751407
Maprs63751407
PheGenIrs63751407
hapmaprs63751407
1000 genomesrs63751407
hgdprs63751407
ensemblrs63751407
gopubmedrs63751407
geneviewrs63751407
scholarrs63751407
googlers63751407
pharmgkbrs63751407
gwascentralrs63751407
openSNPrs63751407
23andMers63751407
23andMe allrs63751407
SNP Nexus

SNPshotrs63751407
SNPdbers63751407
MSV3drs63751407
GWAS Ctlgrs63751407
Max Magnitude0
ClinVar
Risk rs63751407(;)
Alt rs63751407(;)
Reference rs63751407(TC;TC)
Significance Pathogenic
Disease Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome
Variation info
Gene MSH6
CLNDBN Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028175_48028176delTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000009489.3, RCV000074799.3,


[PMID 11245474] MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer.

[PMID 15837969] Molecular analysis of familial endometrial carcinoma: a manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome?

[PMID 17312306] Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.