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

rs587779299

From SNPedia

Orientationplus
Geno Mag Summary
(TGAGAAGATGA;TGAGAAGATGA) 0 common in clinvar
Make rs587779299(-;-)
Make rs587779299(-;TGAGAAGATGA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806619
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs587779299
ebirs587779299
HLIrs587779299
Exacrs587779299
Varsomers587779299
Maprs587779299
PheGenIrs587779299
hapmaprs587779299
1000 genomesrs587779299
hgdprs587779299
ensemblrs587779299
gopubmedrs587779299
geneviewrs587779299
scholarrs587779299
googlers587779299
pharmgkbrs587779299
gwascentralrs587779299
openSNPrs587779299
23andMers587779299
23andMe allrs587779299
SNP Nexus

SNPshotrs587779299
SNPdbers587779299
MSV3drs587779299
GWAS Ctlgrs587779299
Max Magnitude0
ClinVar
Risk rs587779299(;)
Alt rs587779299(;)
Reference rs587779299(TGAGAAGATGA;TGAGAAGATGA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033758_48033768delTGAGAAGATGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074960.2,