rs863224238
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs863224238(-;-) |
Make rs863224238(-;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 7 |
Position | 144623209 |
Gene | TPK1 |
is a | snp |
is | mentioned by |
dbSNP | rs863224238 |
dbSNP (classic) | rs863224238 |
ClinGen | rs863224238 |
ebi | rs863224238 |
HLI | rs863224238 |
Exac | rs863224238 |
Gnomad | rs863224238 |
Varsome | rs863224238 |
LitVar | rs863224238 |
Map | rs863224238 |
PheGenI | rs863224238 |
Biobank | rs863224238 |
1000 genomes | rs863224238 |
hgdp | rs863224238 |
ensembl | rs863224238 |
geneview | rs863224238 |
scholar | rs863224238 |
rs863224238 | |
pharmgkb | rs863224238 |
gwascentral | rs863224238 |
openSNP | rs863224238 |
23andMe | rs863224238 |
SNPshot | rs863224238 |
SNPdbe | rs863224238 |
MSV3d | rs863224238 |
GWAS Ctlg | rs863224238 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224238(-;-) |
Alt | rs863224238(-;-) |
Reference | Rs863224238(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TPK1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000007.13:g.144320302delC |
CLNSRC | |
CLNACC | RCV000197530.1, |