rs72554334
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CTT;CTT) | 0 | common in clinvar |
(D;D) | 0 | |
(I;I) | 0 | common genotype |
Make rs72554334(-;-) |
Make rs72554334(-;CTT) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 38369822 |
Gene | OTC |
is a | snp |
is | mentioned by |
dbSNP | rs72554334 |
dbSNP (classic) | rs72554334 |
ClinGen | rs72554334 |
ebi | rs72554334 |
HLI | rs72554334 |
Exac | rs72554334 |
Gnomad | rs72554334 |
Varsome | rs72554334 |
LitVar | rs72554334 |
Map | rs72554334 |
PheGenI | rs72554334 |
Biobank | rs72554334 |
1000 genomes | rs72554334 |
hgdp | rs72554334 |
ensembl | rs72554334 |
geneview | rs72554334 |
scholar | rs72554334 |
rs72554334 | |
pharmgkb | rs72554334 |
gwascentral | rs72554334 |
openSNP | rs72554334 |
23andMe | rs72554334 |
SNPshot | rs72554334 |
SNPdbe | rs72554334 |
MSV3d | rs72554334 |
GWAS Ctlg | rs72554334 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs72554334(-;-) |
Alt | rs72554334(-;-) |
Reference | Rs72554334(CTT;CTT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | OTC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.38229075_38229077delCTT |
CLNSRC | ClinVar |
CLNACC | RCV000083372.1, |