rs730880392
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs730880392(A;G) |
Make rs730880392(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 15 |
Position | 34792495 |
Gene | ACTC1, LOC101928174 |
is a | snp |
is | mentioned by |
dbSNP | rs730880392 |
dbSNP (classic) | rs730880392 |
ClinGen | rs730880392 |
ebi | rs730880392 |
HLI | rs730880392 |
Exac | rs730880392 |
Gnomad | rs730880392 |
Varsome | rs730880392 |
LitVar | rs730880392 |
Map | rs730880392 |
PheGenI | rs730880392 |
Biobank | rs730880392 |
1000 genomes | rs730880392 |
hgdp | rs730880392 |
ensembl | rs730880392 |
geneview | rs730880392 |
scholar | rs730880392 |
rs730880392 | |
pharmgkb | rs730880392 |
gwascentral | rs730880392 |
openSNP | rs730880392 |
23andMe | rs730880392 |
SNPshot | rs730880392 |
SNPdbe | rs730880392 |
MSV3d | rs730880392 |
GWAS Ctlg | rs730880392 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880392(G;G) |
Alt | rs730880392(G;G) |
Reference | Rs730880392(A;A) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | ACTC1 LOC101928174 RP11-814P5.1 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000015.9:g.35084696T>C |
CLNSRC | |
CLNACC | RCV000223764.1, |