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rs587779295

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779295(-;-)
Make rs587779295(-;T)
Make rs587779295(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806568
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs587779295
ebirs587779295
HLIrs587779295
Exacrs587779295
Varsomers587779295
Maprs587779295
PheGenIrs587779295
hapmaprs587779295
1000 genomesrs587779295
hgdprs587779295
ensemblrs587779295
gopubmedrs587779295
geneviewrs587779295
scholarrs587779295
googlers587779295
pharmgkbrs587779295
gwascentralrs587779295
openSNPrs587779295
23andMers587779295
23andMe allrs587779295
SNP Nexus

SNPshotrs587779295
SNPdbers587779295
MSV3drs587779295
GWAS Ctlgrs587779295
Max Magnitude0
ClinVar
Risk rs587779295(T;T)
Alt rs587779295(T;T)
Reference rs587779295(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033707dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074948.2,