rs199544087
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs199544087(A;A) |
Make rs199544087(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 4 |
Position | 1805761 |
Gene | FGFR3 |
is a | snp |
is | mentioned by |
dbSNP | rs199544087 |
dbSNP (classic) | rs199544087 |
ClinGen | rs199544087 |
ebi | rs199544087 |
HLI | rs199544087 |
Exac | rs199544087 |
Gnomad | rs199544087 |
Varsome | rs199544087 |
LitVar | rs199544087 |
Map | rs199544087 |
PheGenI | rs199544087 |
Biobank | rs199544087 |
1000 genomes | rs199544087 |
hgdp | rs199544087 |
ensembl | rs199544087 |
geneview | rs199544087 |
scholar | rs199544087 |
rs199544087 | |
pharmgkb | rs199544087 |
gwascentral | rs199544087 |
openSNP | rs199544087 |
23andMe | rs199544087 |
SNPshot | rs199544087 |
SNPdbe | rs199544087 |
MSV3d | rs199544087 |
GWAS Ctlg | rs199544087 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199544087(A;A) rs199544087(T;T) |
Alt | rs199544087(A;A) rs199544087(T;T) |
Reference | Rs199544087(G;G) |
Significance | Probable-Pathogenic |
Disease | Myeloproliferative disorder |
Variation | info |
Gene | FGFR3 |
CLNDBN | Myeloproliferative disorder |
Reversed | 0 |
HGVS | NC_000004.11:g.1807488G>A |
CLNSRC | |
CLNACC | RCV000418578.1, |