rs755391236
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs755391236(C;C) |
Make rs755391236(C;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 214997733 |
Gene | ABCA12 |
is a | snp |
is | mentioned by |
dbSNP | rs755391236 |
dbSNP (classic) | rs755391236 |
ClinGen | rs755391236 |
ebi | rs755391236 |
HLI | rs755391236 |
Exac | rs755391236 |
Gnomad | rs755391236 |
Varsome | rs755391236 |
LitVar | rs755391236 |
Map | rs755391236 |
PheGenI | rs755391236 |
Biobank | rs755391236 |
1000 genomes | rs755391236 |
hgdp | rs755391236 |
ensembl | rs755391236 |
geneview | rs755391236 |
scholar | rs755391236 |
rs755391236 | |
pharmgkb | rs755391236 |
gwascentral | rs755391236 |
openSNP | rs755391236 |
23andMe | rs755391236 |
SNPshot | rs755391236 |
SNPdbe | rs755391236 |
MSV3d | rs755391236 |
GWAS Ctlg | rs755391236 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs755391236(A;A) rs755391236(C;C) |
Alt | rs755391236(A;A) rs755391236(C;C) |
Reference | Rs755391236(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.215862457T>A |
CLNSRC | |
CLNACC | RCV000254841.1, |