rs7500834
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
(T;T) | 0 | common in clinvar |
Make rs7500834(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 16178813 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs7500834 |
dbSNP (classic) | rs7500834 |
ClinGen | rs7500834 |
ebi | rs7500834 |
HLI | rs7500834 |
Exac | rs7500834 |
Gnomad | rs7500834 |
Varsome | rs7500834 |
LitVar | rs7500834 |
Map | rs7500834 |
PheGenI | rs7500834 |
Biobank | rs7500834 |
1000 genomes | rs7500834 |
hgdp | rs7500834 |
ensembl | rs7500834 |
geneview | rs7500834 |
scholar | rs7500834 |
rs7500834 | |
pharmgkb | rs7500834 |
gwascentral | rs7500834 |
openSNP | rs7500834 |
23andMe | rs7500834 |
SNPshot | rs7500834 |
SNPdbe | rs7500834 |
MSV3d | rs7500834 |
GWAS Ctlg | rs7500834 |
GMAF | 0.0202 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | Rs7500834(C;C) |
Alt | Rs7500834(C;C) |
Reference | Rs7500834(T;T) |
Significance | Untested |
Disease | |
Variation | info |
Gene | |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000016.9:g.16272670T>C |
CLNSRC | |
CLNACC |