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rs587779143

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779143(A;A)
Make rs587779143(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47478352
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779143
ebirs587779143
HLIrs587779143
Exacrs587779143
Varsomers587779143
Maprs587779143
PheGenIrs587779143
hapmaprs587779143
1000 genomesrs587779143
hgdprs587779143
ensemblrs587779143
gopubmedrs587779143
geneviewrs587779143
scholarrs587779143
googlers587779143
pharmgkbrs587779143
gwascentralrs587779143
openSNPrs587779143
23andMers587779143
23andMe allrs587779143
SNP Nexus

SNPshotrs587779143
SNPdbers587779143
MSV3drs587779143
GWAS Ctlgrs587779143
Max Magnitude0
ClinVar
Risk rs587779143(A;A)
Alt rs587779143(A;A)
Reference rs587779143(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705491G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076450.2,