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rs587779208

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779208(A;A)
Make rs587779208(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799176
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779208
ebirs587779208
HLIrs587779208
Exacrs587779208
Varsomers587779208
Maprs587779208
PheGenIrs587779208
hapmaprs587779208
1000 genomesrs587779208
hgdprs587779208
ensemblrs587779208
gopubmedrs587779208
geneviewrs587779208
scholarrs587779208
googlers587779208
pharmgkbrs587779208
gwascentralrs587779208
openSNPrs587779208
23andMers587779208
23andMe allrs587779208
SNP Nexus

SNPshotrs587779208
SNPdbers587779208
MSV3drs587779208
GWAS Ctlgrs587779208
Max Magnitude0
ClinVar
Risk rs587779208(A;A)
Alt rs587779208(A;A)
Reference rs587779208(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026315T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074641.2,