rs201150384
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 rs201150384(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 71435397 |
Gene | DHCR7 |
is a | snp |
is | mentioned by |
dbSNP | rs201150384 |
dbSNP (classic) | rs201150384 |
ClinGen | rs201150384 |
ebi | rs201150384 |
HLI | rs201150384 |
Exac | rs201150384 |
Gnomad | rs201150384 |
Varsome | rs201150384 |
LitVar | rs201150384 |
Map | rs201150384 |
PheGenI | rs201150384 |
Biobank | rs201150384 |
1000 genomes | rs201150384 |
hgdp | rs201150384 |
ensembl | rs201150384 |
geneview | rs201150384 |
scholar | rs201150384 |
rs201150384 | |
pharmgkb | rs201150384 |
gwascentral | rs201150384 |
openSNP | rs201150384 |
23andMe | rs201150384 |
SNPshot | rs201150384 |
SNPdbe | rs201150384 |
MSV3d | rs201150384 |
GWAS Ctlg | rs201150384 |
Max Magnitude | 3 |