rs373121544
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
Make rs373121544(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 71439040 |
Gene | DHCR7 |
is a | snp |
is | mentioned by |
dbSNP | rs373121544 |
dbSNP (classic) | rs373121544 |
ClinGen | rs373121544 |
ebi | rs373121544 |
HLI | rs373121544 |
Exac | rs373121544 |
Gnomad | rs373121544 |
Varsome | rs373121544 |
LitVar | rs373121544 |
Map | rs373121544 |
PheGenI | rs373121544 |
Biobank | rs373121544 |
1000 genomes | rs373121544 |
hgdp | rs373121544 |
ensembl | rs373121544 |
geneview | rs373121544 |
scholar | rs373121544 |
rs373121544 | |
pharmgkb | rs373121544 |
gwascentral | rs373121544 |
openSNP | rs373121544 |
23andMe | rs373121544 |
SNPshot | rs373121544 |
SNPdbe | rs373121544 |
MSV3d | rs373121544 |
GWAS Ctlg | rs373121544 |
Max Magnitude | 3 |