rs753960624
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common/normal |
(A;G) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
Make rs753960624(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 71441383 |
Gene | DHCR7 |
is a | snp |
is | mentioned by |
dbSNP | rs753960624 |
dbSNP (classic) | rs753960624 |
ClinGen | rs753960624 |
ebi | rs753960624 |
HLI | rs753960624 |
Exac | rs753960624 |
Gnomad | rs753960624 |
Varsome | rs753960624 |
LitVar | rs753960624 |
Map | rs753960624 |
PheGenI | rs753960624 |
Biobank | rs753960624 |
1000 genomes | rs753960624 |
hgdp | rs753960624 |
ensembl | rs753960624 |
geneview | rs753960624 |
scholar | rs753960624 |
rs753960624 | |
pharmgkb | rs753960624 |
gwascentral | rs753960624 |
openSNP | rs753960624 |
23andMe | rs753960624 |
SNPshot | rs753960624 |
SNPdbe | rs753960624 |
MSV3d | rs753960624 |
GWAS Ctlg | rs753960624 |
Max Magnitude | 3 |