rs114863111
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs114863111(A;A) |
Make rs114863111(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 214987734 |
Gene | ABCA12 |
is a | snp |
is | mentioned by |
dbSNP | rs114863111 |
dbSNP (classic) | rs114863111 |
ClinGen | rs114863111 |
ebi | rs114863111 |
HLI | rs114863111 |
Exac | rs114863111 |
Gnomad | rs114863111 |
Varsome | rs114863111 |
LitVar | rs114863111 |
Map | rs114863111 |
PheGenI | rs114863111 |
Biobank | rs114863111 |
1000 genomes | rs114863111 |
hgdp | rs114863111 |
ensembl | rs114863111 |
geneview | rs114863111 |
scholar | rs114863111 |
rs114863111 | |
pharmgkb | rs114863111 |
gwascentral | rs114863111 |
openSNP | rs114863111 |
23andMe | rs114863111 |
SNPshot | rs114863111 |
SNPdbe | rs114863111 |
MSV3d | rs114863111 |
GWAS Ctlg | rs114863111 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs114863111(A;A) rs114863111(T;T) |
Alt | rs114863111(A;A) rs114863111(T;T) |
Reference | Rs114863111(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.215852458G>A |
CLNSRC | |
CLNACC | RCV000255106.1, |