rs387906576
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TGGA;TGGA) | 0 | common in clinvar |
Make rs387906576(-;-) |
Make rs387906576(-;TGGA) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 63482666 |
Gene | ACE |
is a | snp |
is | mentioned by |
dbSNP | rs387906576 |
dbSNP (classic) | rs387906576 |
ClinGen | rs387906576 |
ebi | rs387906576 |
HLI | rs387906576 |
Exac | rs387906576 |
Gnomad | rs387906576 |
Varsome | rs387906576 |
LitVar | rs387906576 |
Map | rs387906576 |
PheGenI | rs387906576 |
Biobank | rs387906576 |
1000 genomes | rs387906576 |
hgdp | rs387906576 |
ensembl | rs387906576 |
geneview | rs387906576 |
scholar | rs387906576 |
rs387906576 | |
pharmgkb | rs387906576 |
gwascentral | rs387906576 |
openSNP | rs387906576 |
23andMe | rs387906576 |
SNPshot | rs387906576 |
SNPdbe | rs387906576 |
MSV3d | rs387906576 |
GWAS Ctlg | rs387906576 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906576(-;-) |
Alt | rs387906576(-;-) |
Reference | Rs387906576(TGGA;TGGA) |
Significance | Pathogenic |
Disease | Renal dysplasia |
Variation | info |
Gene | ACE |
CLNDBN | Renal dysplasia |
Reversed | 0 |
HGVS | NC_000017.10:g.61560027_61560030delTGGA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019687.27, |