rs759514548
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs759514548(G;T) |
Make rs759514548(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 16000168 |
Gene | TTC19, ZSWIM7 |
is a | snp |
is | mentioned by |
dbSNP | rs759514548 |
dbSNP (classic) | rs759514548 |
ClinGen | rs759514548 |
ebi | rs759514548 |
HLI | rs759514548 |
Exac | rs759514548 |
Gnomad | rs759514548 |
Varsome | rs759514548 |
LitVar | rs759514548 |
Map | rs759514548 |
PheGenI | rs759514548 |
Biobank | rs759514548 |
1000 genomes | rs759514548 |
hgdp | rs759514548 |
ensembl | rs759514548 |
geneview | rs759514548 |
scholar | rs759514548 |
rs759514548 | |
pharmgkb | rs759514548 |
gwascentral | rs759514548 |
openSNP | rs759514548 |
23andMe | rs759514548 |
SNPshot | rs759514548 |
SNPdbe | rs759514548 |
MSV3d | rs759514548 |
GWAS Ctlg | rs759514548 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759514548(T;T) |
Alt | rs759514548(T;T) |
Reference | Rs759514548(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TTC19 ZSWIM7 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.15903482G>T |
CLNSRC | |
CLNACC | RCV000200180.1, |