rs483352913
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs483352913(A;A) |
Make rs483352913(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 15 |
Position | 58621471 |
Gene | ADAM10 |
is a | snp |
is | mentioned by |
dbSNP | rs483352913 |
dbSNP (classic) | rs483352913 |
ClinGen | rs483352913 |
ebi | rs483352913 |
HLI | rs483352913 |
Exac | rs483352913 |
Gnomad | rs483352913 |
Varsome | rs483352913 |
LitVar | rs483352913 |
Map | rs483352913 |
PheGenI | rs483352913 |
Biobank | rs483352913 |
1000 genomes | rs483352913 |
hgdp | rs483352913 |
ensembl | rs483352913 |
geneview | rs483352913 |
scholar | rs483352913 |
rs483352913 | |
pharmgkb | rs483352913 |
gwascentral | rs483352913 |
openSNP | rs483352913 |
23andMe | rs483352913 |
SNPshot | rs483352913 |
SNPdbe | rs483352913 |
MSV3d | rs483352913 |
GWAS Ctlg | rs483352913 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs483352913(A;A) |
Alt | rs483352913(A;A) |
Reference | Rs483352913(G;G) |
Significance | Pathogenic |
Disease | Reticulate acropigmentation of Kitamura |
Variation | info |
Gene | ADAM10 |
CLNDBN | Reticulate acropigmentation of Kitamura |
Reversed | 1 |
HGVS | NC_000015.9:g.58913670C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000074428.3, |