rs536394774
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 rs536394774(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 71441308 |
Gene | DHCR7 |
is a | snp |
is | mentioned by |
dbSNP | rs536394774 |
dbSNP (classic) | rs536394774 |
ClinGen | rs536394774 |
ebi | rs536394774 |
HLI | rs536394774 |
Exac | rs536394774 |
Gnomad | rs536394774 |
Varsome | rs536394774 |
LitVar | rs536394774 |
Map | rs536394774 |
PheGenI | rs536394774 |
Biobank | rs536394774 |
1000 genomes | rs536394774 |
hgdp | rs536394774 |
ensembl | rs536394774 |
geneview | rs536394774 |
scholar | rs536394774 |
rs536394774 | |
pharmgkb | rs536394774 |
gwascentral | rs536394774 |
openSNP | rs536394774 |
23andMe | rs536394774 |
SNPshot | rs536394774 |
SNPdbe | rs536394774 |
MSV3d | rs536394774 |
GWAS Ctlg | rs536394774 |
Max Magnitude | 3 |