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

rs587779279

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779279(A;A)
Make rs587779279(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806203
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779279
ebirs587779279
HLIrs587779279
Exacrs587779279
Varsomers587779279
Maprs587779279
PheGenIrs587779279
hapmaprs587779279
1000 genomesrs587779279
hgdprs587779279
ensemblrs587779279
gopubmedrs587779279
geneviewrs587779279
scholarrs587779279
googlers587779279
pharmgkbrs587779279
gwascentralrs587779279
openSNPrs587779279
23andMers587779279
23andMe allrs587779279
SNP Nexus

SNPshotrs587779279
SNPdbers587779279
MSV3drs587779279
GWAS Ctlgrs587779279
Max Magnitude0
ClinVar
Risk rs587779279(A;A)
Alt rs587779279(A;A)
Reference rs587779279(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033342G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074902.3,