rs876657641
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs876657641(A;A) |
Make rs876657641(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 70033470 |
Gene | EDA |
is a | snp |
is | mentioned by |
dbSNP | rs876657641 |
dbSNP (classic) | rs876657641 |
ClinGen | rs876657641 |
ebi | rs876657641 |
HLI | rs876657641 |
Exac | rs876657641 |
Gnomad | rs876657641 |
Varsome | rs876657641 |
LitVar | rs876657641 |
Map | rs876657641 |
PheGenI | rs876657641 |
Biobank | rs876657641 |
1000 genomes | rs876657641 |
hgdp | rs876657641 |
ensembl | rs876657641 |
geneview | rs876657641 |
scholar | rs876657641 |
rs876657641 | |
pharmgkb | rs876657641 |
gwascentral | rs876657641 |
openSNP | rs876657641 |
23andMe | rs876657641 |
SNPshot | rs876657641 |
SNPdbe | rs876657641 |
MSV3d | rs876657641 |
GWAS Ctlg | rs876657641 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876657641(A;A) |
Alt | rs876657641(A;A) |
Reference | Rs876657641(G;G) |
Significance | Probable-Pathogenic |
Disease | Tooth agenesis |
Variation | info |
Gene | EDA |
CLNDBN | Tooth agenesis, selective, X-linked, 1 |
Reversed | 0 |
HGVS | NC_000023.10:g.69253320G>A |
CLNSRC | |
CLNACC | RCV000223248.1, |