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rs587779975

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs587779975(-;-)
Make rs587779975(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412454
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779975
ebirs587779975
HLIrs587779975
Exacrs587779975
Varsomers587779975
Maprs587779975
PheGenIrs587779975
hapmaprs587779975
1000 genomesrs587779975
hgdprs587779975
ensemblrs587779975
gopubmedrs587779975
geneviewrs587779975
scholarrs587779975
googlers587779975
pharmgkbrs587779975
gwascentralrs587779975
openSNPrs587779975
23andMers587779975
23andMe allrs587779975
SNP Nexus

SNPshotrs587779975
SNPdbers587779975
MSV3drs587779975
GWAS Ctlgrs587779975
Max Magnitude0
ClinVar
Risk rs587779975(;)
Alt rs587779975(;)
Reference rs587779975(AA;AA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47639593_47639594delAA
CLNSRC
CLNACC RCV000115539.2,