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rs587779175

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779175(-;-)
Make rs587779175(-;A)
Make rs587779175(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47403262
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779175
ebirs587779175
HLIrs587779175
Exacrs587779175
Varsomers587779175
Maprs587779175
PheGenIrs587779175
hapmaprs587779175
1000 genomesrs587779175
hgdprs587779175
ensemblrs587779175
gopubmedrs587779175
geneviewrs587779175
scholarrs587779175
googlers587779175
pharmgkbrs587779175
gwascentralrs587779175
openSNPrs587779175
23andMers587779175
23andMe allrs587779175
SNP Nexus

SNPshotrs587779175
SNPdbers587779175
MSV3drs587779175
GWAS Ctlgrs587779175
Max Magnitude0
ClinVar
Risk rs587779175(A;A)
Alt rs587779175(A;A)
Reference rs587779175(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630401dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076691.2,