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rs587779105

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779105(-;-)
Make rs587779105(-;A)
Make rs587779105(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47471005
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779105
ebirs587779105
HLIrs587779105
Exacrs587779105
Varsomers587779105
Maprs587779105
PheGenIrs587779105
hapmaprs587779105
1000 genomesrs587779105
hgdprs587779105
ensemblrs587779105
gopubmedrs587779105
geneviewrs587779105
scholarrs587779105
googlers587779105
pharmgkbrs587779105
gwascentralrs587779105
openSNPrs587779105
23andMers587779105
23andMe allrs587779105
SNP Nexus

SNPshotrs587779105
SNPdbers587779105
MSV3drs587779105
GWAS Ctlgrs587779105
Max Magnitude0
ClinVar
Risk rs587779105(A;A)
Alt rs587779105(A;A)
Reference rs587779105(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698144dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076253.2,