rs753966933
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs753966933(A;A) |
Make rs753966933(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 55228708 |
Gene | RAB27A |
is a | snp |
is | mentioned by |
dbSNP | rs753966933 |
dbSNP (classic) | rs753966933 |
ClinGen | rs753966933 |
ebi | rs753966933 |
HLI | rs753966933 |
Exac | rs753966933 |
Gnomad | rs753966933 |
Varsome | rs753966933 |
LitVar | rs753966933 |
Map | rs753966933 |
PheGenI | rs753966933 |
Biobank | rs753966933 |
1000 genomes | rs753966933 |
hgdp | rs753966933 |
ensembl | rs753966933 |
geneview | rs753966933 |
scholar | rs753966933 |
rs753966933 | |
pharmgkb | rs753966933 |
gwascentral | rs753966933 |
openSNP | rs753966933 |
23andMe | rs753966933 |
SNPshot | rs753966933 |
SNPdbe | rs753966933 |
MSV3d | rs753966933 |
GWAS Ctlg | rs753966933 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs753966933(A;A) |
Alt | rs753966933(A;A) |
Reference | Rs753966933(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | RAB27A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.55520906G>A |
CLNSRC | |
CLNACC | RCV000483557.1, |