rs796051979
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs796051979(A;A) |
Make rs796051979(A;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 119759862 |
Gene | HMGCS2 |
is a | snp |
is | mentioned by |
dbSNP | rs796051979 |
dbSNP (classic) | rs796051979 |
ClinGen | rs796051979 |
ebi | rs796051979 |
HLI | rs796051979 |
Exac | rs796051979 |
Gnomad | rs796051979 |
Varsome | rs796051979 |
LitVar | rs796051979 |
Map | rs796051979 |
PheGenI | rs796051979 |
Biobank | rs796051979 |
1000 genomes | rs796051979 |
hgdp | rs796051979 |
ensembl | rs796051979 |
geneview | rs796051979 |
scholar | rs796051979 |
rs796051979 | |
pharmgkb | rs796051979 |
gwascentral | rs796051979 |
openSNP | rs796051979 |
23andMe | rs796051979 |
SNPshot | rs796051979 |
SNPdbe | rs796051979 |
MSV3d | rs796051979 |
GWAS Ctlg | rs796051979 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051979(A;A) |
Alt | rs796051979(A;A) |
Reference | Rs796051979(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | HMGCS2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000001.10:g.120302485A>T |
CLNSRC | |
CLNACC | RCV000185974.2, |