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rs587779232

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779232(A;A)
Make rs587779232(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800110
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779232
ebirs587779232
HLIrs587779232
Exacrs587779232
Varsomers587779232
Maprs587779232
PheGenIrs587779232
hapmaprs587779232
1000 genomesrs587779232
hgdprs587779232
ensemblrs587779232
gopubmedrs587779232
geneviewrs587779232
scholarrs587779232
googlers587779232
pharmgkbrs587779232
gwascentralrs587779232
openSNPrs587779232
23andMers587779232
23andMe allrs587779232
SNP Nexus

SNPshotrs587779232
SNPdbers587779232
MSV3drs587779232
GWAS Ctlgrs587779232
Max Magnitude0
ClinVar
Risk rs587779232(A;A)
Alt rs587779232(A;A)
Reference rs587779232(T;T)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027249T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074719.2, RCV000130308.2,