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rs587781870

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs587781870(-;-)
Make rs587781870(-;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803445
GeneMSH6
is asnp
is mentioned by
dbSNPrs587781870
ebirs587781870
HLIrs587781870
Exacrs587781870
Varsomers587781870
Maprs587781870
PheGenIrs587781870
hapmaprs587781870
1000 genomesrs587781870
hgdprs587781870
ensemblrs587781870
gopubmedrs587781870
geneviewrs587781870
scholarrs587781870
googlers587781870
pharmgkbrs587781870
gwascentralrs587781870
openSNPrs587781870
23andMers587781870
23andMe allrs587781870
SNP Nexus

SNPshotrs587781870
SNPdbers587781870
MSV3drs587781870
GWAS Ctlgrs587781870
Max Magnitude0
ClinVar
Risk rs587781870(;)
Alt rs587781870(;)
Reference rs587781870(TA;TA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48030584_48030585delTA
CLNSRC
CLNACC RCV000130192.2,