rs730880420
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs730880420(C;C) |
Make rs730880420(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 8745662 |
Gene | CAV3, SSUH2 |
is a | snp |
is | mentioned by |
dbSNP | rs730880420 |
dbSNP (classic) | rs730880420 |
ClinGen | rs730880420 |
ebi | rs730880420 |
HLI | rs730880420 |
Exac | rs730880420 |
Gnomad | rs730880420 |
Varsome | rs730880420 |
LitVar | rs730880420 |
Map | rs730880420 |
PheGenI | rs730880420 |
Biobank | rs730880420 |
1000 genomes | rs730880420 |
hgdp | rs730880420 |
ensembl | rs730880420 |
geneview | rs730880420 |
scholar | rs730880420 |
rs730880420 | |
pharmgkb | rs730880420 |
gwascentral | rs730880420 |
openSNP | rs730880420 |
23andMe | rs730880420 |
SNPshot | rs730880420 |
SNPdbe | rs730880420 |
MSV3d | rs730880420 |
GWAS Ctlg | rs730880420 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880420(C;C) |
Alt | rs730880420(C;C) |
Reference | Rs730880420(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SSUH2 CAV3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.8787348T>C |
CLNSRC | |
CLNACC | RCV000157836.1, |