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rs587776704

From SNPedia

Merged intors63751407
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;TC) 6 Lynch syndrome, pathogenic mutation
(TC;TC) 0 common in clinvar


Make rs587776704(-;-)
ReferenceGRCh38 38.1/142
Chromosome2
Position47801036
GeneMSH6
is asnp
is mentioned by
dbSNPrs587776704
dbSNP (classic)rs587776704
ClinGenrs587776704
ebirs587776704
HLIrs587776704
Exacrs587776704
Gnomadrs587776704
Varsomers587776704
LitVarrs587776704
Maprs587776704
PheGenIrs587776704
Biobankrs587776704
1000 genomesrs587776704
hgdprs587776704
ensemblrs587776704
geneviewrs587776704
scholarrs587776704
googlers587776704
pharmgkbrs587776704
gwascentralrs587776704
openSNPrs587776704
23andMers587776704
SNPshotrs587776704
SNPdbers587776704
MSV3drs587776704
GWAS Ctlgrs587776704
StatusMerged into rs63751407
Max Magnitude6
ClinVar
Risk
Alt
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,