rs11861980
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs11861980(A;A) |
Make rs11861980(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 16173376 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs11861980 |
dbSNP (classic) | rs11861980 |
ClinGen | rs11861980 |
ebi | rs11861980 |
HLI | rs11861980 |
Exac | rs11861980 |
Gnomad | rs11861980 |
Varsome | rs11861980 |
LitVar | rs11861980 |
Map | rs11861980 |
PheGenI | rs11861980 |
Biobank | rs11861980 |
1000 genomes | rs11861980 |
hgdp | rs11861980 |
ensembl | rs11861980 |
geneview | rs11861980 |
scholar | rs11861980 |
rs11861980 | |
pharmgkb | rs11861980 |
gwascentral | rs11861980 |
openSNP | rs11861980 |
23andMe | rs11861980 |
SNPshot | rs11861980 |
SNPdbe | rs11861980 |
MSV3d | rs11861980 |
GWAS Ctlg | rs11861980 |
GMAF | 0.003214 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs11861980(A;A) rs11861980(C;C) |
Alt | rs11861980(A;A) rs11861980(C;C) |
Reference | Rs11861980(G;G) |
Significance | Untested |
Disease | |
Variation | info |
Gene | ABCC6 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000016.9:g.16267233G>C |
CLNSRC | |
CLNACC |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
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