rs773134475
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
(G;G) | 0 | common/normal |
Make rs773134475(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 71435613 |
Gene | DHCR7 |
is a | snp |
is | mentioned by |
dbSNP | rs773134475 |
dbSNP (classic) | rs773134475 |
ClinGen | rs773134475 |
ebi | rs773134475 |
HLI | rs773134475 |
Exac | rs773134475 |
Gnomad | rs773134475 |
Varsome | rs773134475 |
LitVar | rs773134475 |
Map | rs773134475 |
PheGenI | rs773134475 |
Biobank | rs773134475 |
1000 genomes | rs773134475 |
hgdp | rs773134475 |
ensembl | rs773134475 |
geneview | rs773134475 |
scholar | rs773134475 |
rs773134475 | |
pharmgkb | rs773134475 |
gwascentral | rs773134475 |
openSNP | rs773134475 |
23andMe | rs773134475 |
SNPshot | rs773134475 |
SNPdbe | rs773134475 |
MSV3d | rs773134475 |
GWAS Ctlg | rs773134475 |
Max Magnitude | 3 |