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rs587779198

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779198(A;G)
Make rs587779198(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47416294
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779198
ebirs587779198
HLIrs587779198
Exacrs587779198
Varsomers587779198
Maprs587779198
PheGenIrs587779198
hapmaprs587779198
1000 genomesrs587779198
hgdprs587779198
ensemblrs587779198
gopubmedrs587779198
geneviewrs587779198
scholarrs587779198
googlers587779198
pharmgkbrs587779198
gwascentralrs587779198
openSNPrs587779198
23andMers587779198
23andMe allrs587779198
SNP Nexus

SNPshotrs587779198
SNPdbers587779198
MSV3drs587779198
GWAS Ctlgrs587779198
Max Magnitude0
ClinVar
Risk rs587779198(G;G)
Alt rs587779198(G;G)
Reference rs587779198(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643433A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076759.2,