Have questions? Visit https://www.reddit.com/r/SNPedia

rs587782562

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782562(-;-)
Make rs587782562(-;AATG)
Make rs587782562(AATG;AATG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803577
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782562
ebirs587782562
HLIrs587782562
Exacrs587782562
Varsomers587782562
Maprs587782562
PheGenIrs587782562
hapmaprs587782562
1000 genomesrs587782562
hgdprs587782562
ensemblrs587782562
gopubmedrs587782562
geneviewrs587782562
scholarrs587782562
googlers587782562
pharmgkbrs587782562
gwascentralrs587782562
openSNPrs587782562
23andMers587782562
23andMe allrs587782562
SNP Nexus

SNPshotrs587782562
SNPdbers587782562
MSV3drs587782562
GWAS Ctlgrs587782562
Max Magnitude0
ClinVar
Risk rs587782562(AATG;AATG)
Alt rs587782562(AATG;AATG)
Reference rs587782562(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome not provided Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030718_48030721dupATGA
CLNSRC
CLNACC RCV000131783.2, RCV000202177.1, RCV000221780.1, RCV000233414.1,