rs1001916923
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1001916923(A;G) |
Make rs1001916923(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 21908147 |
Gene | ABCC9 |
is a | snp |
is | mentioned by |
dbSNP | rs1001916923 |
dbSNP (classic) | rs1001916923 |
ClinGen | rs1001916923 |
ebi | rs1001916923 |
HLI | rs1001916923 |
Exac | rs1001916923 |
Gnomad | rs1001916923 |
Varsome | rs1001916923 |
LitVar | rs1001916923 |
Map | rs1001916923 |
PheGenI | rs1001916923 |
Biobank | rs1001916923 |
1000 genomes | rs1001916923 |
hgdp | rs1001916923 |
ensembl | rs1001916923 |
geneview | rs1001916923 |
scholar | rs1001916923 |
rs1001916923 | |
pharmgkb | rs1001916923 |
gwascentral | rs1001916923 |
openSNP | rs1001916923 |
23andMe | rs1001916923 |
SNPshot | rs1001916923 |
SNPdbe | rs1001916923 |
MSV3d | rs1001916923 |
GWAS Ctlg | rs1001916923 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1001916923(G;G) rs1001916923(T;T) |
Alt | rs1001916923(G;G) rs1001916923(T;T) |
Reference | Rs1001916923(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.22061081A>G |
CLNSRC | |
CLNACC | RCV000486887.1, |