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

rs587779246

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779246(C;T)
Make rs587779246(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800747
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779246
ebirs587779246
HLIrs587779246
Exacrs587779246
Varsomers587779246
Maprs587779246
PheGenIrs587779246
hapmaprs587779246
1000 genomesrs587779246
hgdprs587779246
ensemblrs587779246
gopubmedrs587779246
geneviewrs587779246
scholarrs587779246
googlers587779246
pharmgkbrs587779246
gwascentralrs587779246
openSNPrs587779246
23andMers587779246
23andMe allrs587779246
SNP Nexus

SNPshotrs587779246
SNPdbers587779246
MSV3drs587779246
GWAS Ctlgrs587779246
Max Magnitude0
ClinVar
Risk rs587779246(T;T)
Alt rs587779246(T;T)
Reference rs587779246(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027886C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074779.2,