rs758503371
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs758503371(C;T) |
Make rs758503371(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 12896333 |
Gene | GCDH |
is a | snp |
is | mentioned by |
dbSNP | rs758503371 |
dbSNP (classic) | rs758503371 |
ClinGen | rs758503371 |
ebi | rs758503371 |
HLI | rs758503371 |
Exac | rs758503371 |
Gnomad | rs758503371 |
Varsome | rs758503371 |
LitVar | rs758503371 |
Map | rs758503371 |
PheGenI | rs758503371 |
Biobank | rs758503371 |
1000 genomes | rs758503371 |
hgdp | rs758503371 |
ensembl | rs758503371 |
geneview | rs758503371 |
scholar | rs758503371 |
rs758503371 | |
pharmgkb | rs758503371 |
gwascentral | rs758503371 |
openSNP | rs758503371 |
23andMe | rs758503371 |
SNPshot | rs758503371 |
SNPdbe | rs758503371 |
MSV3d | rs758503371 |
GWAS Ctlg | rs758503371 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs758503371(T;T) |
Alt | rs758503371(T;T) |
Reference | Rs758503371(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GCDH |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.13007147C>T |
CLNSRC | |
CLNACC | RCV000416219.1, |