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rs587779296

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779296(-;-)
Make rs587779296(-;ATCTCCCA)
Make rs587779296(ATCTCCCA;ATCTCCCA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806577
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs587779296
ebirs587779296
HLIrs587779296
Exacrs587779296
Varsomers587779296
Maprs587779296
PheGenIrs587779296
hapmaprs587779296
1000 genomesrs587779296
hgdprs587779296
ensemblrs587779296
gopubmedrs587779296
geneviewrs587779296
scholarrs587779296
googlers587779296
pharmgkbrs587779296
gwascentralrs587779296
openSNPrs587779296
23andMers587779296
23andMe allrs587779296
SNP Nexus

SNPshotrs587779296
SNPdbers587779296
MSV3drs587779296
GWAS Ctlgrs587779296
Max Magnitude0
ClinVar
Risk rs587779296(AATCTCCC;AATCTCCC)
Alt rs587779296(AATCTCCC;AATCTCCC)
Reference rs587779296(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033709_48033716dupATCTCCCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074949.2,