Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779964

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779964(-;-)
Make rs587779964(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47471047
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779964
ebirs587779964
HLIrs587779964
Exacrs587779964
Varsomers587779964
Maprs587779964
PheGenIrs587779964
hapmaprs587779964
1000 genomesrs587779964
hgdprs587779964
ensemblrs587779964
gopubmedrs587779964
geneviewrs587779964
scholarrs587779964
googlers587779964
pharmgkbrs587779964
gwascentralrs587779964
openSNPrs587779964
23andMers587779964
23andMe allrs587779964
SNP Nexus

SNPshotrs587779964
SNPdbers587779964
MSV3drs587779964
GWAS Ctlgrs587779964
Max Magnitude0
ClinVar
Risk rs587779964(;)
Alt rs587779964(;)
Reference rs587779964(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47698186delG
CLNSRC
CLNACC RCV000115509.2,