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rs587779226

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779226(-;-)
Make rs587779226(-;CT)
Make rs587779226(CT;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800034
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779226
ebirs587779226
HLIrs587779226
Exacrs587779226
Varsomers587779226
Maprs587779226
PheGenIrs587779226
hapmaprs587779226
1000 genomesrs587779226
hgdprs587779226
ensemblrs587779226
gopubmedrs587779226
geneviewrs587779226
scholarrs587779226
googlers587779226
pharmgkbrs587779226
gwascentralrs587779226
openSNPrs587779226
23andMers587779226
23andMe allrs587779226
SNP Nexus

SNPshotrs587779226
SNPdbers587779226
MSV3drs587779226
GWAS Ctlgrs587779226
Max Magnitude0
ClinVar
Risk rs587779226(CT;CT)
Alt rs587779226(CT;CT)
Reference rs587779226(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027172_48027173dupCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074707.2,