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

rs751033488

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs751033488(-;-)
Make rs751033488(-;TCAG)
Make rs751033488(TCAG;TCAG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806630
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs751033488
ebirs751033488
HLIrs751033488
Exacrs751033488
Varsomers751033488
Maprs751033488
PheGenIrs751033488
hapmaprs751033488
1000 genomesrs751033488
hgdprs751033488
ensemblrs751033488
gopubmedrs751033488
geneviewrs751033488
scholarrs751033488
googlers751033488
pharmgkbrs751033488
gwascentralrs751033488
openSNPrs751033488
23andMers751033488
23andMe allrs751033488
SNP Nexus

SNPshotrs751033488
SNPdbers751033488
MSV3drs751033488
GWAS Ctlgrs751033488
Max Magnitude0
ClinVar
Risk rs751033488(TCAG;TCAG)
Alt rs751033488(TCAG;TCAG)
Reference rs751033488(;)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48033773_48033776dupGTCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074964.3, RCV000131963.4, RCV000202165.1,