rs139625465
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs139625465(G;T) |
Make rs139625465(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 19 |
Position | 7932691 |
Gene | TIMM44 |
is a | snp |
is | mentioned by |
dbSNP | rs139625465 |
dbSNP (classic) | rs139625465 |
ClinGen | rs139625465 |
ebi | rs139625465 |
HLI | rs139625465 |
Exac | rs139625465 |
Gnomad | rs139625465 |
Varsome | rs139625465 |
LitVar | rs139625465 |
Map | rs139625465 |
PheGenI | rs139625465 |
Biobank | rs139625465 |
1000 genomes | rs139625465 |
hgdp | rs139625465 |
ensembl | rs139625465 |
geneview | rs139625465 |
scholar | rs139625465 |
rs139625465 | |
pharmgkb | rs139625465 |
gwascentral | rs139625465 |
openSNP | rs139625465 |
23andMe | rs139625465 |
SNPshot | rs139625465 |
SNPdbe | rs139625465 |
MSV3d | rs139625465 |
GWAS Ctlg | rs139625465 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139625465(A;A) rs139625465(T;T) |
Alt | rs139625465(A;A) rs139625465(T;T) |
Reference | Rs139625465(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TIMM44 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.7997576G>T |
CLNSRC | |
CLNACC | RCV000198581.2, |