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rs1064797084

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome11
Position128810657
GeneFLI1
is asnp
is mentioned by
dbSNPrs1064797084
dbSNP (old)rs1064797084
ClinGenrs1064797084
ebirs1064797084
HLIrs1064797084
Exacrs1064797084
Gnomadrs1064797084
Varsomers1064797084
Maprs1064797084
PheGenIrs1064797084
Biobankrs1064797084
1000 genomesrs1064797084
hgdprs1064797084
ensemblrs1064797084
gopubmedrs1064797084
geneviewrs1064797084
scholarrs1064797084
googlers1064797084
pharmgkbrs1064797084
gwascentralrs1064797084
openSNPrs1064797084
23andMers1064797084
23andMe allrs1064797084
SNPshotrs1064797084
SNPdbers1064797084
MSV3drs1064797084
GWAS Ctlgrs1064797084
Max Magnitude0
ClinVar
Risk rs1064797084(G;G)
Alt rs1064797084(G;G)
Reference Rs1064797084(A;A)
Significance Pathogenic
Disease Bleeding disorder
Variation info
Gene FLI1
CLNDBN Bleeding disorder, platelet-type, 21
Reversed 0
HGVS NC_000011.9:g.128680552A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000487469.1,