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rs63750262

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750262(-;-)
Make rs63750262(-;AATG)
Make rs63750262(AATG;AATG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806474
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs63750262
ebirs63750262
HLIrs63750262
Exacrs63750262
Varsomers63750262
Maprs63750262
PheGenIrs63750262
hapmaprs63750262
1000 genomesrs63750262
hgdprs63750262
ensemblrs63750262
gopubmedrs63750262
geneviewrs63750262
scholarrs63750262
googlers63750262
pharmgkbrs63750262
gwascentralrs63750262
openSNPrs63750262
23andMers63750262
23andMe allrs63750262
SNP Nexus

SNPshotrs63750262
SNPdbers63750262
MSV3drs63750262
GWAS Ctlgrs63750262
Max Magnitude0
ClinVar
Risk rs63750262(AATG;AATG)
Alt rs63750262(AATG;AATG)
Reference rs63750262(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033610_48033613dupAATG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074939.2,