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

rs587782275

From SNPedia

Orientationplus
Geno Mag Summary
(CAGT;CAGT) 0 common in clinvar
Make rs587782275(-;-)
Make rs587782275(-;CAGT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800130
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782275
ebirs587782275
HLIrs587782275
Exacrs587782275
Varsomers587782275
Maprs587782275
PheGenIrs587782275
hapmaprs587782275
1000 genomesrs587782275
hgdprs587782275
ensemblrs587782275
gopubmedrs587782275
geneviewrs587782275
scholarrs587782275
googlers587782275
pharmgkbrs587782275
gwascentralrs587782275
openSNPrs587782275
23andMers587782275
23andMe allrs587782275
SNP Nexus

SNPshotrs587782275
SNPdbers587782275
MSV3drs587782275
GWAS Ctlgrs587782275
Max Magnitude0
ClinVar
Risk rs587782275(;)
Alt rs587782275(;)
Reference rs587782275(CAGT;CAGT)
Significance 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.48027272_48027275delTCAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074720.2, RCV000162408.2, RCV000202111.2,