rs730880445
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs730880445(A;A) |
Make rs730880445(A;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | X |
Position | 101401674 |
Gene | GLA, RPL36A-HNRNPH2 |
is a | snp |
is | mentioned by |
dbSNP | rs730880445 |
dbSNP (classic) | rs730880445 |
ClinGen | rs730880445 |
ebi | rs730880445 |
HLI | rs730880445 |
Exac | rs730880445 |
Gnomad | rs730880445 |
Varsome | rs730880445 |
LitVar | rs730880445 |
Map | rs730880445 |
PheGenI | rs730880445 |
Biobank | rs730880445 |
1000 genomes | rs730880445 |
hgdp | rs730880445 |
ensembl | rs730880445 |
geneview | rs730880445 |
scholar | rs730880445 |
rs730880445 | |
pharmgkb | rs730880445 |
gwascentral | rs730880445 |
openSNP | rs730880445 |
23andMe | rs730880445 |
SNPshot | rs730880445 |
SNPdbe | rs730880445 |
MSV3d | rs730880445 |
GWAS Ctlg | rs730880445 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880445(A;A) |
Alt | rs730880445(A;A) |
Reference | Rs730880445(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | RPL36A-HNRNPH2 GLA |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.100656662A>T |
CLNSRC | |
CLNACC | RCV000157891.1, |