rs727503009
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs727503009(A;T) |
Make rs727503009(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 70033521 |
Gene | EDA |
is a | snp |
is | mentioned by |
dbSNP | rs727503009 |
dbSNP (classic) | rs727503009 |
ClinGen | rs727503009 |
ebi | rs727503009 |
HLI | rs727503009 |
Exac | rs727503009 |
Gnomad | rs727503009 |
Varsome | rs727503009 |
LitVar | rs727503009 |
Map | rs727503009 |
PheGenI | rs727503009 |
Biobank | rs727503009 |
1000 genomes | rs727503009 |
hgdp | rs727503009 |
ensembl | rs727503009 |
geneview | rs727503009 |
scholar | rs727503009 |
rs727503009 | |
pharmgkb | rs727503009 |
gwascentral | rs727503009 |
openSNP | rs727503009 |
23andMe | rs727503009 |
SNPshot | rs727503009 |
SNPdbe | rs727503009 |
MSV3d | rs727503009 |
GWAS Ctlg | rs727503009 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs727503009(G;G) rs727503009(T;T) |
Alt | rs727503009(G;G) rs727503009(T;T) |
Reference | Rs727503009(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | EDA |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000023.10:g.69253371A>G; NC_000023.10:g.69253371A>T |
CLNSRC | |
CLNACC | RCV000478625.1, RCV000150604.1, |