rs1064797085
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AATT;AATT) | 0 | common in clinvar |
Chromosome | 11 |
Position | 128810621 |
Gene | FLI1 |
is a | snp |
is | mentioned by |
dbSNP | rs1064797085 |
dbSNP (classic) | rs1064797085 |
ClinGen | rs1064797085 |
ebi | rs1064797085 |
HLI | rs1064797085 |
Exac | rs1064797085 |
Gnomad | rs1064797085 |
Varsome | rs1064797085 |
LitVar | rs1064797085 |
Map | rs1064797085 |
PheGenI | rs1064797085 |
Biobank | rs1064797085 |
1000 genomes | rs1064797085 |
hgdp | rs1064797085 |
ensembl | rs1064797085 |
geneview | rs1064797085 |
scholar | rs1064797085 |
rs1064797085 | |
pharmgkb | rs1064797085 |
gwascentral | rs1064797085 |
openSNP | rs1064797085 |
23andMe | rs1064797085 |
SNPshot | rs1064797085 |
SNPdbe | rs1064797085 |
MSV3d | rs1064797085 |
GWAS Ctlg | rs1064797085 |
Max Magnitude | 0 |
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, |