rs61750426
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs61750426(-;-) |
Make rs61750426(-;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 7 |
Position | 92494497 |
Gene | GATAD1, PEX1 |
is a | snp |
is | mentioned by |
dbSNP | rs61750426 |
dbSNP (classic) | rs61750426 |
ClinGen | rs61750426 |
ebi | rs61750426 |
HLI | rs61750426 |
Exac | rs61750426 |
Gnomad | rs61750426 |
Varsome | rs61750426 |
LitVar | rs61750426 |
Map | rs61750426 |
PheGenI | rs61750426 |
Biobank | rs61750426 |
1000 genomes | rs61750426 |
hgdp | rs61750426 |
ensembl | rs61750426 |
geneview | rs61750426 |
scholar | rs61750426 |
rs61750426 | |
pharmgkb | rs61750426 |
gwascentral | rs61750426 |
openSNP | rs61750426 |
23andMe | rs61750426 |
SNPshot | rs61750426 |
SNPdbe | rs61750426 |
MSV3d | rs61750426 |
GWAS Ctlg | rs61750426 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61750426(-;-) |
Alt | rs61750426(-;-) |
Reference | Rs61750426(A;A) |
Significance | Other |
Disease | Zellweger syndrome Peroxisome biogenesis disorder 11A Peroxisome biogenesis disorder 11B Peroxisome biogenesis disorder 1B not provided |
Variation | info |
Gene | PEX1 |
CLNDBN | Zellweger syndrome Peroxisome biogenesis disorder 11A Peroxisome biogenesis disorder 11B Peroxisome biogenesis disorder 1B not provided |
Reversed | 1 |
HGVS | NC_000007.13:g.92123811delT |
CLNSRC | |
CLNACC | RCV000169435.2, RCV000270718.1, RCV000328074.1, RCV000362944.1, RCV000414630.1, |