rs797045905
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs797045905(G;G) |
Make rs797045905(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 135164629 |
Gene | RAB3GAP1, ZRANB3 |
is a | snp |
is | mentioned by |
dbSNP | rs797045905 |
dbSNP (classic) | rs797045905 |
ClinGen | rs797045905 |
ebi | rs797045905 |
HLI | rs797045905 |
Exac | rs797045905 |
Gnomad | rs797045905 |
Varsome | rs797045905 |
LitVar | rs797045905 |
Map | rs797045905 |
PheGenI | rs797045905 |
Biobank | rs797045905 |
1000 genomes | rs797045905 |
hgdp | rs797045905 |
ensembl | rs797045905 |
geneview | rs797045905 |
scholar | rs797045905 |
rs797045905 | |
pharmgkb | rs797045905 |
gwascentral | rs797045905 |
openSNP | rs797045905 |
23andMe | rs797045905 |
SNPshot | rs797045905 |
SNPdbe | rs797045905 |
MSV3d | rs797045905 |
GWAS Ctlg | rs797045905 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797045905(G;G) |
Alt | rs797045905(G;G) |
Reference | Rs797045905(T;T) |
Significance | Pathogenic |
Disease | Warburg micro syndrome 1 |
Variation | info |
Gene | RAB3GAP1 |
CLNDBN | Warburg micro syndrome 1 |
Reversed | 0 |
HGVS | NC_000002.11:g.135922199T>G |
CLNSRC | |
CLNACC | RCV000194301.1, |