rs202166915
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs202166915(A;A) |
Make rs202166915(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 19355710 |
Gene | PDHA1 |
is a | snp |
is | mentioned by |
dbSNP | rs202166915 |
dbSNP (classic) | rs202166915 |
ClinGen | rs202166915 |
ebi | rs202166915 |
HLI | rs202166915 |
Exac | rs202166915 |
Gnomad | rs202166915 |
Varsome | rs202166915 |
LitVar | rs202166915 |
Map | rs202166915 |
PheGenI | rs202166915 |
Biobank | rs202166915 |
1000 genomes | rs202166915 |
hgdp | rs202166915 |
ensembl | rs202166915 |
geneview | rs202166915 |
scholar | rs202166915 |
rs202166915 | |
pharmgkb | rs202166915 |
gwascentral | rs202166915 |
openSNP | rs202166915 |
23andMe | rs202166915 |
SNPshot | rs202166915 |
SNPdbe | rs202166915 |
MSV3d | rs202166915 |
GWAS Ctlg | rs202166915 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs202166915(A;A) |
Alt | rs202166915(A;A) |
Reference | Rs202166915(G;G) |
Significance | Probable-Pathogenic |
Disease | Inborn genetic diseases not specified |
Variation | info |
Gene | PDHA1 |
CLNDBN | Inborn genetic diseases not specified |
Reversed | 0 |
HGVS | NC_000023.10:g.19373828G>A |
CLNSRC | |
CLNACC | RCV000190809.1, RCV000200145.2, |