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rs1064797083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome11
Position128810638
GeneFLI1
is asnp
is mentioned by
dbSNPrs1064797083
dbSNP (old)rs1064797083
ClinGenrs1064797083
ebirs1064797083
HLIrs1064797083
Exacrs1064797083
Gnomadrs1064797083
Varsomers1064797083
LitVarrs1064797083
Maprs1064797083
PheGenIrs1064797083
Biobankrs1064797083
1000 genomesrs1064797083
hgdprs1064797083
ensemblrs1064797083
gopubmedrs1064797083
geneviewrs1064797083
scholarrs1064797083
googlers1064797083
pharmgkbrs1064797083
gwascentralrs1064797083
openSNPrs1064797083
23andMers1064797083
23andMe allrs1064797083
SNPshotrs1064797083
SNPdbers1064797083
MSV3drs1064797083
GWAS Ctlgrs1064797083
Max Magnitude0
ClinVar
Risk rs1064797083(T;T)
Alt rs1064797083(T;T)
Reference Rs1064797083(C;C)
Significance Pathogenic
Disease Bleeding disorder
Variation info
Gene FLI1
CLNDBN Bleeding disorder, platelet-type, 21
Reversed 0
HGVS NC_000011.9:g.128680533C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000487466.1,