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rs1064797085

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AATT;AATT) 0 common in clinvar
Chromosome11
Position128810621
GeneFLI1
is asnp
is mentioned by
dbSNPrs1064797085
dbSNP (old)rs1064797085
ClinGenrs1064797085
ebirs1064797085
HLIrs1064797085
Exacrs1064797085
Gnomadrs1064797085
Varsomers1064797085
Maprs1064797085
PheGenIrs1064797085
Biobankrs1064797085
1000 genomesrs1064797085
hgdprs1064797085
ensemblrs1064797085
gopubmedrs1064797085
geneviewrs1064797085
scholarrs1064797085
googlers1064797085
pharmgkbrs1064797085
gwascentralrs1064797085
openSNPrs1064797085
23andMers1064797085
23andMe allrs1064797085
SNPshotrs1064797085
SNPdbers1064797085
MSV3drs1064797085
GWAS Ctlgrs1064797085
Max Magnitude0
ClinVar
Risk rs1064797085(-;-)
Alt rs1064797085(-;-)
Reference Rs1064797085(AATT;AATT)
Significance Pathogenic
Disease Bleeding disorder
Variation info
Gene FLI1
CLNDBN Bleeding disorder, platelet-type, 21
Reversed 0
HGVS NC_000011.9:g.128680516_128680519delATTA
CLNSRC OMIM Allelic Variant
CLNACC RCV000487462.1,