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rs773148506

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773148506(C;T)
Make rs773148506(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position128810599
GeneFLI1
is asnp
is mentioned by
dbSNPrs773148506
ebirs773148506
HLIrs773148506
Exacrs773148506
Varsomers773148506
Maprs773148506
PheGenIrs773148506
hapmaprs773148506
1000 genomesrs773148506
hgdprs773148506
ensemblrs773148506
gopubmedrs773148506
geneviewrs773148506
scholarrs773148506
googlers773148506
pharmgkbrs773148506
gwascentralrs773148506
openSNPrs773148506
23andMers773148506
23andMe allrs773148506
SNP Nexus

SNPshotrs773148506
SNPdbers773148506
MSV3drs773148506
GWAS Ctlgrs773148506
Max Magnitude0
ClinVar
Risk rs773148506(A,T;A,T)
Alt rs773148506(A,T;A,T)
Reference rs773148506(C;C)
Significance Pathogenic
Disease Bleeding disorder platelet type macrothrombocytopenia
Variation info
Gene FLI1
CLNDBN Bleeding disorder platelet type macrothrombocytopenia
Reversed 0
HGVS NC_000011.9:g.128680494C>T
CLNSRC University of Sydney
CLNACC RCV000197145.1,