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rs587779073

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779073(-;-)
Make rs587779073(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47429764
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779073
ebirs587779073
HLIrs587779073
Exacrs587779073
Varsomers587779073
Maprs587779073
PheGenIrs587779073
hapmaprs587779073
1000 genomesrs587779073
hgdprs587779073
ensemblrs587779073
gopubmedrs587779073
geneviewrs587779073
scholarrs587779073
googlers587779073
pharmgkbrs587779073
gwascentralrs587779073
openSNPrs587779073
23andMers587779073
23andMe allrs587779073
SNP Nexus

SNPshotrs587779073
SNPdbers587779073
MSV3drs587779073
GWAS Ctlgrs587779073
Max Magnitude0
ClinVar
Risk rs587779073(;)
Alt rs587779073(;)
Reference rs587779073(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656903delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076039.2,