rs1133577
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1133577(G;T) |
Make rs1133577(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 75073944 |
Gene | ABCB7 |
is a | snp |
is | mentioned by |
dbSNP | rs1133577 |
dbSNP (classic) | rs1133577 |
ClinGen | rs1133577 |
ebi | rs1133577 |
HLI | rs1133577 |
Exac | rs1133577 |
Gnomad | rs1133577 |
Varsome | rs1133577 |
LitVar | rs1133577 |
Map | rs1133577 |
PheGenI | rs1133577 |
Biobank | rs1133577 |
1000 genomes | rs1133577 |
hgdp | rs1133577 |
ensembl | rs1133577 |
geneview | rs1133577 |
scholar | rs1133577 |
rs1133577 | |
pharmgkb | rs1133577 |
gwascentral | rs1133577 |
openSNP | rs1133577 |
23andMe | rs1133577 |
SNPshot | rs1133577 |
SNPdbe | rs1133577 |
MSV3d | rs1133577 |
GWAS Ctlg | rs1133577 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1133577(A;A) rs1133577(T;T) |
Alt | rs1133577(A;A) rs1133577(T;T) |
Reference | Rs1133577(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCB7 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.74293779C>T |
CLNSRC | |
CLNACC | RCV000199533.2, |