rs35426403
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs35426403(C;C) |
Make rs35426403(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 2408720 |
Gene | PEX10 |
is a | snp |
is | mentioned by |
dbSNP | rs35426403 |
dbSNP (classic) | rs35426403 |
ClinGen | rs35426403 |
ebi | rs35426403 |
HLI | rs35426403 |
Exac | rs35426403 |
Gnomad | rs35426403 |
Varsome | rs35426403 |
LitVar | rs35426403 |
Map | rs35426403 |
PheGenI | rs35426403 |
Biobank | rs35426403 |
1000 genomes | rs35426403 |
hgdp | rs35426403 |
ensembl | rs35426403 |
geneview | rs35426403 |
scholar | rs35426403 |
rs35426403 | |
pharmgkb | rs35426403 |
gwascentral | rs35426403 |
openSNP | rs35426403 |
23andMe | rs35426403 |
SNPshot | rs35426403 |
SNPdbe | rs35426403 |
MSV3d | rs35426403 |
GWAS Ctlg | rs35426403 |
GMAF | 0.006428 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs35426403(C;C) |
Alt | rs35426403(C;C) |
Reference | Rs35426403(T;T) |
Significance | Untested |
Disease | |
Variation | info |
Gene | PEX10 |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000001.10:g.2340159A>G |
CLNSRC | |
CLNACC |