rs35082957
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs35082957(A;A) |
Make rs35082957(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 2406553 |
Gene | PEX10 |
is a | snp |
is | mentioned by |
dbSNP | rs35082957 |
dbSNP (classic) | rs35082957 |
ClinGen | rs35082957 |
ebi | rs35082957 |
HLI | rs35082957 |
Exac | rs35082957 |
Gnomad | rs35082957 |
Varsome | rs35082957 |
LitVar | rs35082957 |
Map | rs35082957 |
PheGenI | rs35082957 |
Biobank | rs35082957 |
1000 genomes | rs35082957 |
hgdp | rs35082957 |
ensembl | rs35082957 |
geneview | rs35082957 |
scholar | rs35082957 |
rs35082957 | |
pharmgkb | rs35082957 |
gwascentral | rs35082957 |
openSNP | rs35082957 |
23andMe | rs35082957 |
SNPshot | rs35082957 |
SNPdbe | rs35082957 |
MSV3d | rs35082957 |
GWAS Ctlg | rs35082957 |
GMAF | 0.003214 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs35082957(A;A) |
Alt | rs35082957(A;A) |
Reference | Rs35082957(G;G) |
Significance | Non-pathogenic |
Disease | not specified Zellweger syndrome |
Variation | info |
Gene | PEX10 |
CLNDBN | not specified Zellweger syndrome |
Reversed | 1 |
HGVS | NC_000001.10:g.2337992C>T |
CLNSRC | Illumina |
CLNACC | RCV000247875.1, RCV000282889.1, |