rs754645487
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs754645487(A;A) |
Make rs754645487(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 122462103 |
Gene | HTRA1, LOC105378525 |
is a | snp |
is | mentioned by |
dbSNP | rs754645487 |
dbSNP (classic) | rs754645487 |
ClinGen | rs754645487 |
ebi | rs754645487 |
HLI | rs754645487 |
Exac | rs754645487 |
Gnomad | rs754645487 |
Varsome | rs754645487 |
LitVar | rs754645487 |
Map | rs754645487 |
PheGenI | rs754645487 |
Biobank | rs754645487 |
1000 genomes | rs754645487 |
hgdp | rs754645487 |
ensembl | rs754645487 |
geneview | rs754645487 |
scholar | rs754645487 |
rs754645487 | |
pharmgkb | rs754645487 |
gwascentral | rs754645487 |
openSNP | rs754645487 |
23andMe | rs754645487 |
SNPshot | rs754645487 |
SNPdbe | rs754645487 |
MSV3d | rs754645487 |
GWAS Ctlg | rs754645487 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs754645487(A;A) rs754645487(T;T) |
Alt | rs754645487(A;A) rs754645487(T;T) |
Reference | Rs754645487(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | HTRA1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.124221619C>T |
CLNSRC | |
CLNACC | RCV000487710.1, |