rs368927897
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs368927897(G;T) |
Make rs368927897(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 5072541 |
Gene | INSL6, JAK2 |
is a | snp |
is | mentioned by |
dbSNP | rs368927897 |
dbSNP (classic) | rs368927897 |
ClinGen | rs368927897 |
ebi | rs368927897 |
HLI | rs368927897 |
Exac | rs368927897 |
Gnomad | rs368927897 |
Varsome | rs368927897 |
LitVar | rs368927897 |
Map | rs368927897 |
PheGenI | rs368927897 |
Biobank | rs368927897 |
1000 genomes | rs368927897 |
hgdp | rs368927897 |
ensembl | rs368927897 |
geneview | rs368927897 |
scholar | rs368927897 |
rs368927897 | |
pharmgkb | rs368927897 |
gwascentral | rs368927897 |
openSNP | rs368927897 |
23andMe | rs368927897 |
SNPshot | rs368927897 |
SNPdbe | rs368927897 |
MSV3d | rs368927897 |
GWAS Ctlg | rs368927897 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs368927897(T;T) |
Alt | rs368927897(T;T) |
Reference | Rs368927897(G;G) |
Significance | Probable-Pathogenic |
Disease | Myeloproliferative disorder |
Variation | info |
Gene | JAK2 |
CLNDBN | Myeloproliferative disorder |
Reversed | 0 |
HGVS | NC_000009.11:g.5072541G>T |
CLNSRC | |
CLNACC | RCV000418120.1, |