rs114149656
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs114149656(C;T) |
Make rs114149656(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 16188935 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs114149656 |
dbSNP (classic) | rs114149656 |
ClinGen | rs114149656 |
ebi | rs114149656 |
HLI | rs114149656 |
Exac | rs114149656 |
Gnomad | rs114149656 |
Varsome | rs114149656 |
LitVar | rs114149656 |
Map | rs114149656 |
PheGenI | rs114149656 |
Biobank | rs114149656 |
1000 genomes | rs114149656 |
hgdp | rs114149656 |
ensembl | rs114149656 |
geneview | rs114149656 |
scholar | rs114149656 |
rs114149656 | |
pharmgkb | rs114149656 |
gwascentral | rs114149656 |
openSNP | rs114149656 |
23andMe | rs114149656 |
SNPshot | rs114149656 |
SNPdbe | rs114149656 |
MSV3d | rs114149656 |
GWAS Ctlg | rs114149656 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs114149656(A;A) rs114149656(T;T) |
Alt | rs114149656(A;A) rs114149656(T;T) |
Reference | Rs114149656(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCC6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.16282792C>A |
CLNSRC | |
CLNACC | RCV000424143.1, |