rs199503269
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs199503269(A;A) |
Make rs199503269(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 214937608 |
Gene | ABCA12, LOC101928103 |
is a | snp |
is | mentioned by |
dbSNP | rs199503269 |
dbSNP (classic) | rs199503269 |
ClinGen | rs199503269 |
ebi | rs199503269 |
HLI | rs199503269 |
Exac | rs199503269 |
Gnomad | rs199503269 |
Varsome | rs199503269 |
LitVar | rs199503269 |
Map | rs199503269 |
PheGenI | rs199503269 |
Biobank | rs199503269 |
1000 genomes | rs199503269 |
hgdp | rs199503269 |
ensembl | rs199503269 |
geneview | rs199503269 |
scholar | rs199503269 |
rs199503269 | |
pharmgkb | rs199503269 |
gwascentral | rs199503269 |
openSNP | rs199503269 |
23andMe | rs199503269 |
SNPshot | rs199503269 |
SNPdbe | rs199503269 |
MSV3d | rs199503269 |
GWAS Ctlg | rs199503269 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199503269(A;A) |
Alt | rs199503269(A;A) |
Reference | Rs199503269(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | LOC101928103 ABCA12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.215802332G>A |
CLNSRC | |
CLNACC | RCV000480311.1, |