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rs587779063

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779063(A;T)
Make rs587779063(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47416353
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779063
ebirs587779063
HLIrs587779063
Exacrs587779063
Varsomers587779063
Maprs587779063
PheGenIrs587779063
hapmaprs587779063
1000 genomesrs587779063
hgdprs587779063
ensemblrs587779063
gopubmedrs587779063
geneviewrs587779063
scholarrs587779063
googlers587779063
pharmgkbrs587779063
gwascentralrs587779063
openSNPrs587779063
23andMers587779063
23andMe allrs587779063
SNP Nexus

SNPshotrs587779063
SNPdbers587779063
MSV3drs587779063
GWAS Ctlgrs587779063
Max Magnitude0
ClinVar
Risk rs587779063(T;T)
Alt rs587779063(T;T)
Reference rs587779063(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643492A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075993.2,