rs768913919
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs768913919(C;T) |
Make rs768913919(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 158111415 |
Gene | SERAC1 |
is a | snp |
is | mentioned by |
dbSNP | rs768913919 |
dbSNP (classic) | rs768913919 |
ClinGen | rs768913919 |
ebi | rs768913919 |
HLI | rs768913919 |
Exac | rs768913919 |
Gnomad | rs768913919 |
Varsome | rs768913919 |
LitVar | rs768913919 |
Map | rs768913919 |
PheGenI | rs768913919 |
Biobank | rs768913919 |
1000 genomes | rs768913919 |
hgdp | rs768913919 |
ensembl | rs768913919 |
geneview | rs768913919 |
scholar | rs768913919 |
rs768913919 | |
pharmgkb | rs768913919 |
gwascentral | rs768913919 |
openSNP | rs768913919 |
23andMe | rs768913919 |
SNPshot | rs768913919 |
SNPdbe | rs768913919 |
MSV3d | rs768913919 |
GWAS Ctlg | rs768913919 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768913919(G;G) rs768913919(T;T) |
Alt | rs768913919(G;G) rs768913919(T;T) |
Reference | Rs768913919(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SERAC1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.158532447C>G |
CLNSRC | |
CLNACC | RCV000197976.2, |