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rs587782281

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782281(-;-)
Make rs587782281(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47796013
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782281
ebirs587782281
HLIrs587782281
Exacrs587782281
Varsomers587782281
Maprs587782281
PheGenIrs587782281
hapmaprs587782281
1000 genomesrs587782281
hgdprs587782281
ensemblrs587782281
gopubmedrs587782281
geneviewrs587782281
scholarrs587782281
googlers587782281
pharmgkbrs587782281
gwascentralrs587782281
openSNPrs587782281
23andMers587782281
23andMe allrs587782281
SNP Nexus

SNPshotrs587782281
SNPdbers587782281
MSV3drs587782281
GWAS Ctlgrs587782281
Max Magnitude0
ClinVar
Risk rs587782281(;)
Alt rs587782281(;)
Reference rs587782281(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48023153delT
CLNSRC
CLNACC RCV000162426.2, RCV000231303.1,