rs756771290
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs756771290(C;C) |
Make rs756771290(C;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 215007788 |
Gene | ABCA12 |
is a | snp |
is | mentioned by |
dbSNP | rs756771290 |
dbSNP (classic) | rs756771290 |
ClinGen | rs756771290 |
ebi | rs756771290 |
HLI | rs756771290 |
Exac | rs756771290 |
Gnomad | rs756771290 |
Varsome | rs756771290 |
LitVar | rs756771290 |
Map | rs756771290 |
PheGenI | rs756771290 |
Biobank | rs756771290 |
1000 genomes | rs756771290 |
hgdp | rs756771290 |
ensembl | rs756771290 |
geneview | rs756771290 |
scholar | rs756771290 |
rs756771290 | |
pharmgkb | rs756771290 |
gwascentral | rs756771290 |
openSNP | rs756771290 |
23andMe | rs756771290 |
SNPshot | rs756771290 |
SNPdbe | rs756771290 |
MSV3d | rs756771290 |
GWAS Ctlg | rs756771290 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs756771290(C;C) |
Alt | rs756771290(C;C) |
Reference | Rs756771290(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.215872512T>C |
CLNSRC | |
CLNACC | RCV000255774.1, |