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rs1064797087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome11
Position128810662
GeneFLI1
is asnp
is mentioned by
dbSNPrs1064797087
dbSNP (old)rs1064797087
ClinGenrs1064797087
ebirs1064797087
HLIrs1064797087
Exacrs1064797087
Gnomadrs1064797087
Varsomers1064797087
Maprs1064797087
PheGenIrs1064797087
Biobankrs1064797087
1000 genomesrs1064797087
hgdprs1064797087
ensemblrs1064797087
gopubmedrs1064797087
geneviewrs1064797087
scholarrs1064797087
googlers1064797087
pharmgkbrs1064797087
gwascentralrs1064797087
openSNPrs1064797087
23andMers1064797087
23andMe allrs1064797087
SNPshotrs1064797087
SNPdbers1064797087
MSV3drs1064797087
GWAS Ctlgrs1064797087
Max Magnitude0
ClinVar
Risk rs1064797087(G;G)
Alt rs1064797087(G;G)
Reference Rs1064797087(A;A)
Significance Pathogenic
Disease Bleeding disorder
Variation info
Gene FLI1
CLNDBN Bleeding disorder, platelet-type, 21
Reversed 0
HGVS NC_000011.9:g.128680557A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000487460.1,