rs775773057
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 rs775773057(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 71439028 |
Gene | DHCR7 |
is a | snp |
is | mentioned by |
dbSNP | rs775773057 |
dbSNP (classic) | rs775773057 |
ClinGen | rs775773057 |
ebi | rs775773057 |
HLI | rs775773057 |
Exac | rs775773057 |
Gnomad | rs775773057 |
Varsome | rs775773057 |
LitVar | rs775773057 |
Map | rs775773057 |
PheGenI | rs775773057 |
Biobank | rs775773057 |
1000 genomes | rs775773057 |
hgdp | rs775773057 |
ensembl | rs775773057 |
geneview | rs775773057 |
scholar | rs775773057 |
rs775773057 | |
pharmgkb | rs775773057 |
gwascentral | rs775773057 |
openSNP | rs775773057 |
23andMe | rs775773057 |
SNPshot | rs775773057 |
SNPdbe | rs775773057 |
MSV3d | rs775773057 |
GWAS Ctlg | rs775773057 |
Max Magnitude | 3 |