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rs587781650

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781650(-;-)
Make rs587781650(-;T)
Make rs587781650(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800108
GeneMSH6
is asnp
is mentioned by
dbSNPrs587781650
ebirs587781650
HLIrs587781650
Exacrs587781650
Varsomers587781650
Maprs587781650
PheGenIrs587781650
hapmaprs587781650
1000 genomesrs587781650
hgdprs587781650
ensemblrs587781650
gopubmedrs587781650
geneviewrs587781650
scholarrs587781650
googlers587781650
pharmgkbrs587781650
gwascentralrs587781650
openSNPrs587781650
23andMers587781650
23andMe allrs587781650
SNP Nexus

SNPshotrs587781650
SNPdbers587781650
MSV3drs587781650
GWAS Ctlgrs587781650
Max Magnitude0
ClinVar
Risk rs587781650(T;T)
Alt rs587781650(T;T)
Reference rs587781650(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027247dupT
CLNSRC
CLNACC RCV000129782.2,