rs863224147
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs863224147(C;T) |
Make rs863224147(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 19359612 |
Gene | MAP3K15, PDHA1 |
is a | snp |
is | mentioned by |
dbSNP | rs863224147 |
dbSNP (classic) | rs863224147 |
ClinGen | rs863224147 |
ebi | rs863224147 |
HLI | rs863224147 |
Exac | rs863224147 |
Gnomad | rs863224147 |
Varsome | rs863224147 |
LitVar | rs863224147 |
Map | rs863224147 |
PheGenI | rs863224147 |
Biobank | rs863224147 |
1000 genomes | rs863224147 |
hgdp | rs863224147 |
ensembl | rs863224147 |
geneview | rs863224147 |
scholar | rs863224147 |
rs863224147 | |
pharmgkb | rs863224147 |
gwascentral | rs863224147 |
openSNP | rs863224147 |
23andMe | rs863224147 |
SNPshot | rs863224147 |
SNPdbe | rs863224147 |
MSV3d | rs863224147 |
GWAS Ctlg | rs863224147 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224147(T;T) |
Alt | rs863224147(T;T) |
Reference | Rs863224147(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PDHA1 MAP3K15 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.19377730C>T |
CLNSRC | |
CLNACC | RCV000198575.2, |