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rs587782809

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782809(-;-)
Make rs587782809(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799273
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782809
ebirs587782809
HLIrs587782809
Exacrs587782809
Varsomers587782809
Maprs587782809
PheGenIrs587782809
hapmaprs587782809
1000 genomesrs587782809
hgdprs587782809
ensemblrs587782809
gopubmedrs587782809
geneviewrs587782809
scholarrs587782809
googlers587782809
pharmgkbrs587782809
gwascentralrs587782809
openSNPrs587782809
23andMers587782809
23andMe allrs587782809
SNP Nexus

SNPshotrs587782809
SNPdbers587782809
MSV3drs587782809
GWAS Ctlgrs587782809
Max Magnitude0
ClinVar
Risk rs587782809(;)
Alt rs587782809(;)
Reference rs587782809(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026412delG
CLNSRC
CLNACC RCV000132371.2,