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rs587779301

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779301(-;-)
Make rs587779301(-;ATTTC)
Make rs587779301(ATTTC;ATTTC)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806650
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs587779301
ebirs587779301
HLIrs587779301
Exacrs587779301
Varsomers587779301
Maprs587779301
PheGenIrs587779301
hapmaprs587779301
1000 genomesrs587779301
hgdprs587779301
ensemblrs587779301
gopubmedrs587779301
geneviewrs587779301
scholarrs587779301
googlers587779301
pharmgkbrs587779301
gwascentralrs587779301
openSNPrs587779301
23andMers587779301
23andMe allrs587779301
SNP Nexus

SNPshotrs587779301
SNPdbers587779301
MSV3drs587779301
GWAS Ctlgrs587779301
Max Magnitude0
ClinVar
Risk rs587779301(ATTTC;ATTTC)
Alt rs587779301(ATTTC;ATTTC)
Reference rs587779301(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033785_48033789dupATTTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074966.2,