Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751405(C;C)
Make rs63751405(C;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position47799287
GeneMSH6
is asnp
is mentioned by
dbSNPrs63751405
ebirs63751405
HLIrs63751405
Exacrs63751405
Varsomers63751405
Maprs63751405
PheGenIrs63751405
hapmaprs63751405
1000 genomesrs63751405
hgdprs63751405
ensemblrs63751405
gopubmedrs63751405
geneviewrs63751405
scholarrs63751405
googlers63751405
pharmgkbrs63751405
gwascentralrs63751405
openSNPrs63751405
23andMers63751405
23andMe allrs63751405
SNP Nexus

SNPshotrs63751405
SNPdbers63751405
MSV3drs63751405
GWAS Ctlgrs63751405
Max Magnitude0
ClinVar
Risk rs63751405(C;C)
Alt rs63751405(C;C)
Reference rs63751405(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48026426T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074648.2, RCV000128873.2, RCV000214282.1,