rs267608179
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs267608179(A;A) |
Make rs267608179(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 7 |
Position | 92494486 |
Gene | GATAD1, PEX1 |
is a | snp |
is | mentioned by |
dbSNP | rs267608179 |
dbSNP (classic) | rs267608179 |
ClinGen | rs267608179 |
ebi | rs267608179 |
HLI | rs267608179 |
Exac | rs267608179 |
Gnomad | rs267608179 |
Varsome | rs267608179 |
LitVar | rs267608179 |
Map | rs267608179 |
PheGenI | rs267608179 |
Biobank | rs267608179 |
1000 genomes | rs267608179 |
hgdp | rs267608179 |
ensembl | rs267608179 |
geneview | rs267608179 |
scholar | rs267608179 |
rs267608179 | |
pharmgkb | rs267608179 |
gwascentral | rs267608179 |
openSNP | rs267608179 |
23andMe | rs267608179 |
SNPshot | rs267608179 |
SNPdbe | rs267608179 |
MSV3d | rs267608179 |
GWAS Ctlg | rs267608179 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267608179(A;A) |
Alt | rs267608179(A;A) |
Reference | Rs267608179(G;G) |
Significance | Other |
Disease | Zellweger syndrome |
Variation | info |
Gene | PEX1 |
CLNDBN | Zellweger syndrome |
Reversed | 1 |
HGVS | NC_000007.13:g.92123800C>T |
CLNSRC | |
CLNACC | RCV000169032.2, |