rs113993965
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs113993965(A;A) |
Make rs113993965(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 189808465 |
Gene | TP63 |
is a | snp |
is | mentioned by |
dbSNP | rs113993965 |
dbSNP (classic) | rs113993965 |
ClinGen | rs113993965 |
ebi | rs113993965 |
HLI | rs113993965 |
Exac | rs113993965 |
Gnomad | rs113993965 |
Varsome | rs113993965 |
LitVar | rs113993965 |
Map | rs113993965 |
PheGenI | rs113993965 |
Biobank | rs113993965 |
1000 genomes | rs113993965 |
hgdp | rs113993965 |
ensembl | rs113993965 |
geneview | rs113993965 |
scholar | rs113993965 |
rs113993965 | |
pharmgkb | rs113993965 |
gwascentral | rs113993965 |
openSNP | rs113993965 |
23andMe | rs113993965 |
SNPshot | rs113993965 |
SNPdbe | rs113993965 |
MSV3d | rs113993965 |
GWAS Ctlg | rs113993965 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs113993965(A;A) |
Alt | rs113993965(A;A) |
Reference | Rs113993965(G;G) |
Significance | Pathogenic |
Disease | ADULT syndrome not provided |
Variation | info |
Gene | TP63 |
CLNDBN | ADULT syndrome not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.189526254G>A; NC_000003.11:g.189526254G>T |
CLNSRC | ClinVar GeneReviews |
CLNACC | RCV000032229.1, RCV000494181.1, |