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rs587782425

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782425(-;-)
Make rs587782425(-;C)
Make rs587782425(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803501
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782425
ebirs587782425
HLIrs587782425
Exacrs587782425
Varsomers587782425
Maprs587782425
PheGenIrs587782425
hapmaprs587782425
1000 genomesrs587782425
hgdprs587782425
ensemblrs587782425
gopubmedrs587782425
geneviewrs587782425
scholarrs587782425
googlers587782425
pharmgkbrs587782425
gwascentralrs587782425
openSNPrs587782425
23andMers587782425
23andMe allrs587782425
SNP Nexus

SNPshotrs587782425
SNPdbers587782425
MSV3drs587782425
GWAS Ctlgrs587782425
Max Magnitude0
ClinVar
Risk rs587782425(C;C)
Alt rs587782425(C;C)
Reference rs587782425(;)
Significance Pathogenic
Disease Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48030647dupC
CLNSRC HGMD International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074831.3, RCV000078312.5, RCV000115412.5,