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rs587779189

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779189(-;-)
Make rs587779189(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47414339
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779189
ebirs587779189
HLIrs587779189
Exacrs587779189
Varsomers587779189
Maprs587779189
PheGenIrs587779189
hapmaprs587779189
1000 genomesrs587779189
hgdprs587779189
ensemblrs587779189
gopubmedrs587779189
geneviewrs587779189
scholarrs587779189
googlers587779189
pharmgkbrs587779189
gwascentralrs587779189
openSNPrs587779189
23andMers587779189
23andMe allrs587779189
SNP Nexus

SNPshotrs587779189
SNPdbers587779189
MSV3drs587779189
GWAS Ctlgrs587779189
Max Magnitude0
ClinVar
Risk rs587779189(;)
Alt rs587779189(;)
Reference rs587779189(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641478delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076739.2,