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rs587776704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs587776704(-;-)
Make rs587776704(-;TC)
ReferenceGRCh38 38.1/142
Chromosome2
Position47801036
GeneMSH6
is asnp
is mentioned by
dbSNPrs587776704
ebirs587776704
HLIrs587776704
Exacrs587776704
Varsomers587776704
Maprs587776704
PheGenIrs587776704
hapmaprs587776704
1000 genomesrs587776704
hgdprs587776704
ensemblrs587776704
gopubmedrs587776704
geneviewrs587776704
scholarrs587776704
googlers587776704
pharmgkbrs587776704
gwascentralrs587776704
openSNPrs587776704
23andMers587776704
23andMe allrs587776704
SNP Nexus

SNPshotrs587776704
SNPdbers587776704
MSV3drs587776704
GWAS Ctlgrs587776704
Max Magnitude0
ClinVar
Risk rs587776704(;)
Alt rs587776704(;)
Reference rs587776704(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,