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rs587782862

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782862(-;-)
Make rs587782862(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47801003
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782862
ebirs587782862
HLIrs587782862
Exacrs587782862
Varsomers587782862
Maprs587782862
PheGenIrs587782862
hapmaprs587782862
1000 genomesrs587782862
hgdprs587782862
ensemblrs587782862
gopubmedrs587782862
geneviewrs587782862
scholarrs587782862
googlers587782862
pharmgkbrs587782862
gwascentralrs587782862
openSNPrs587782862
23andMers587782862
23andMe allrs587782862
SNP Nexus

SNPshotrs587782862
SNPdbers587782862
MSV3drs587782862
GWAS Ctlgrs587782862
Max Magnitude0
ClinVar
Risk rs587782862(;)
Alt rs587782862(;)
Reference rs587782862(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.48028142delG
CLNSRC
CLNACC RCV000132481.2,