rs748057401
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs748057401(A;A) |
Make rs748057401(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 119493821 |
Gene | HSD17B4 |
is a | snp |
is | mentioned by |
dbSNP | rs748057401 |
dbSNP (classic) | rs748057401 |
ClinGen | rs748057401 |
ebi | rs748057401 |
HLI | rs748057401 |
Exac | rs748057401 |
Gnomad | rs748057401 |
Varsome | rs748057401 |
LitVar | rs748057401 |
Map | rs748057401 |
PheGenI | rs748057401 |
Biobank | rs748057401 |
1000 genomes | rs748057401 |
hgdp | rs748057401 |
ensembl | rs748057401 |
geneview | rs748057401 |
scholar | rs748057401 |
rs748057401 | |
pharmgkb | rs748057401 |
gwascentral | rs748057401 |
openSNP | rs748057401 |
23andMe | rs748057401 |
SNPshot | rs748057401 |
SNPdbe | rs748057401 |
MSV3d | rs748057401 |
GWAS Ctlg | rs748057401 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs748057401(A;A) |
Alt | rs748057401(A;A) |
Reference | Rs748057401(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | HSD17B4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.118829516G>A |
CLNSRC | |
CLNACC | RCV000493335.1, |