rs387906911
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs387906911(A;A) |
Make rs387906911(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 219218505 |
Gene | ABCB6 |
is a | snp |
is | mentioned by |
dbSNP | rs387906911 |
dbSNP (classic) | rs387906911 |
ClinGen | rs387906911 |
ebi | rs387906911 |
HLI | rs387906911 |
Exac | rs387906911 |
Gnomad | rs387906911 |
Varsome | rs387906911 |
LitVar | rs387906911 |
Map | rs387906911 |
PheGenI | rs387906911 |
Biobank | rs387906911 |
1000 genomes | rs387906911 |
hgdp | rs387906911 |
ensembl | rs387906911 |
geneview | rs387906911 |
scholar | rs387906911 |
rs387906911 | |
pharmgkb | rs387906911 |
gwascentral | rs387906911 |
openSNP | rs387906911 |
23andMe | rs387906911 |
SNPshot | rs387906911 |
SNPdbe | rs387906911 |
MSV3d | rs387906911 |
GWAS Ctlg | rs387906911 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906911(A;A) |
Alt | rs387906911(A;A) |
Reference | Rs387906911(G;G) |
Significance | Pathogenic |
Disease | Microphthalmia |
Variation | info |
Gene | ABCB6 |
CLNDBN | Microphthalmia, isolated, with coloboma 7 |
Reversed | 1 |
HGVS | NC_000002.11:g.220083227C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000023440.2, |