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rs587779173

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779173(A;T)
Make rs587779173(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412453
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779173
ebirs587779173
HLIrs587779173
Exacrs587779173
Varsomers587779173
Maprs587779173
PheGenIrs587779173
hapmaprs587779173
1000 genomesrs587779173
hgdprs587779173
ensemblrs587779173
gopubmedrs587779173
geneviewrs587779173
scholarrs587779173
googlers587779173
pharmgkbrs587779173
gwascentralrs587779173
openSNPrs587779173
23andMers587779173
23andMe allrs587779173
SNP Nexus

SNPshotrs587779173
SNPdbers587779173
MSV3drs587779173
GWAS Ctlgrs587779173
Max Magnitude0
ClinVar
Risk rs587779173(T;T)
Alt rs587779173(T;T)
Reference rs587779173(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639592A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076680.2,