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

rs587779318

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779318(C;T)
Make rs587779318(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47798677
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779318
ebirs587779318
HLIrs587779318
Exacrs587779318
Varsomers587779318
Maprs587779318
PheGenIrs587779318
hapmaprs587779318
1000 genomesrs587779318
hgdprs587779318
ensemblrs587779318
gopubmedrs587779318
geneviewrs587779318
scholarrs587779318
googlers587779318
pharmgkbrs587779318
gwascentralrs587779318
openSNPrs587779318
23andMers587779318
23andMe allrs587779318
SNP Nexus

SNPshotrs587779318
SNPdbers587779318
MSV3drs587779318
GWAS Ctlgrs587779318
Max Magnitude0
ClinVar
Risk rs587779318(T;T)
Alt rs587779318(T;T)
Reference rs587779318(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025816C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075025.2,