Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064797086

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position128810639
GeneFLI1
is asnp
is mentioned by
dbSNPrs1064797086
dbSNP (old)rs1064797086
ClinGenrs1064797086
ebirs1064797086
HLIrs1064797086
Exacrs1064797086
Gnomadrs1064797086
Varsomers1064797086
Maprs1064797086
PheGenIrs1064797086
Biobankrs1064797086
1000 genomesrs1064797086
hgdprs1064797086
ensemblrs1064797086
gopubmedrs1064797086
geneviewrs1064797086
scholarrs1064797086
googlers1064797086
pharmgkbrs1064797086
gwascentralrs1064797086
openSNPrs1064797086
23andMers1064797086
23andMe allrs1064797086
SNPshotrs1064797086
SNPdbers1064797086
MSV3drs1064797086
GWAS Ctlgrs1064797086
Max Magnitude0
ClinVar
Risk rs1064797086(A;A)
Alt rs1064797086(A;A)
Reference Rs1064797086(G;G)
Significance Pathogenic
Disease Bleeding disorder
Variation info
Gene FLI1
CLNDBN Bleeding disorder, platelet-type, 21
Reversed 0
HGVS NC_000011.9:g.128680534G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000487465.1,