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rs63750139

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750139(C;T)
Make rs63750139(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806488
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs63750139
ebirs63750139
HLIrs63750139
Exacrs63750139
Varsomers63750139
Maprs63750139
PheGenIrs63750139
hapmaprs63750139
1000 genomesrs63750139
hgdprs63750139
ensemblrs63750139
gopubmedrs63750139
geneviewrs63750139
scholarrs63750139
googlers63750139
pharmgkbrs63750139
gwascentralrs63750139
openSNPrs63750139
23andMers63750139
23andMe allrs63750139
SNP Nexus

SNPshotrs63750139
SNPdbers63750139
MSV3drs63750139
GWAS Ctlgrs63750139
Max Magnitude0
ClinVar
Risk rs63750139(T;T)
Alt rs63750139(T;T)
Reference rs63750139(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033627C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074940.2,