rs187043152
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs187043152(A;A) |
Make rs187043152(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 105801714 |
Gene | ZFPM2, ZFPM2-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs187043152 |
dbSNP (classic) | rs187043152 |
ClinGen | rs187043152 |
ebi | rs187043152 |
HLI | rs187043152 |
Exac | rs187043152 |
Gnomad | rs187043152 |
Varsome | rs187043152 |
LitVar | rs187043152 |
Map | rs187043152 |
PheGenI | rs187043152 |
Biobank | rs187043152 |
1000 genomes | rs187043152 |
hgdp | rs187043152 |
ensembl | rs187043152 |
geneview | rs187043152 |
scholar | rs187043152 |
rs187043152 | |
pharmgkb | rs187043152 |
gwascentral | rs187043152 |
openSNP | rs187043152 |
23andMe | rs187043152 |
SNPshot | rs187043152 |
SNPdbe | rs187043152 |
MSV3d | rs187043152 |
GWAS Ctlg | rs187043152 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs187043152(A;A) rs187043152(T;T) |
Alt | rs187043152(A;A) rs187043152(T;T) |
Reference | Rs187043152(G;G) |
Significance | Other |
Disease | Tetralogy of Fallot 46 not specified |
Variation | info |
Gene | ZFPM2 ZFPM2-AS1 |
CLNDBN | Tetralogy of Fallot 46,XY sex reversal 9 not specified |
Reversed | 0 |
HGVS | NC_000008.10:g.106813942G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000032716.3, RCV000144723.2, RCV000455350.1, |