rs387906577
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs387906577(-;T) |
Make rs387906577(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 148741145 |
Gene | AGTR1 |
is a | snp |
is | mentioned by |
dbSNP | rs387906577 |
dbSNP (classic) | rs387906577 |
ClinGen | rs387906577 |
ebi | rs387906577 |
HLI | rs387906577 |
Exac | rs387906577 |
Gnomad | rs387906577 |
Varsome | rs387906577 |
LitVar | rs387906577 |
Map | rs387906577 |
PheGenI | rs387906577 |
Biobank | rs387906577 |
1000 genomes | rs387906577 |
hgdp | rs387906577 |
ensembl | rs387906577 |
geneview | rs387906577 |
scholar | rs387906577 |
rs387906577 | |
pharmgkb | rs387906577 |
gwascentral | rs387906577 |
openSNP | rs387906577 |
23andMe | rs387906577 |
SNPshot | rs387906577 |
SNPdbe | rs387906577 |
MSV3d | rs387906577 |
GWAS Ctlg | rs387906577 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906577(T;T) |
Alt | rs387906577(T;T) |
Reference | Rs387906577(-;-) |
Significance | Pathogenic |
Disease | Renal dysplasia |
Variation | info |
Gene | AGTR1 |
CLNDBN | Renal dysplasia |
Reversed | 0 |
HGVS | NC_000003.11:g.148458932dupT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019689.30, |