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

rs587779252

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779252(A;A)
Make rs587779252(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47801003
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779252
ebirs587779252
HLIrs587779252
Exacrs587779252
Varsomers587779252
Maprs587779252
PheGenIrs587779252
hapmaprs587779252
1000 genomesrs587779252
hgdprs587779252
ensemblrs587779252
gopubmedrs587779252
geneviewrs587779252
scholarrs587779252
googlers587779252
pharmgkbrs587779252
gwascentralrs587779252
openSNPrs587779252
23andMers587779252
23andMe allrs587779252
SNP Nexus

SNPshotrs587779252
SNPdbers587779252
MSV3drs587779252
GWAS Ctlgrs587779252
Max Magnitude0
ClinVar
Risk rs587779252(A;A)
Alt rs587779252(A;A)
Reference rs587779252(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028142G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074796.2,