rs765196598
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs765196598(A;A) |
Make rs765196598(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 196247479 |
Gene | PCYT1A |
is a | snp |
is | mentioned by |
dbSNP | rs765196598 |
dbSNP (classic) | rs765196598 |
ClinGen | rs765196598 |
ebi | rs765196598 |
HLI | rs765196598 |
Exac | rs765196598 |
Gnomad | rs765196598 |
Varsome | rs765196598 |
LitVar | rs765196598 |
Map | rs765196598 |
PheGenI | rs765196598 |
Biobank | rs765196598 |
1000 genomes | rs765196598 |
hgdp | rs765196598 |
ensembl | rs765196598 |
geneview | rs765196598 |
scholar | rs765196598 |
rs765196598 | |
pharmgkb | rs765196598 |
gwascentral | rs765196598 |
openSNP | rs765196598 |
23andMe | rs765196598 |
SNPshot | rs765196598 |
SNPdbe | rs765196598 |
MSV3d | rs765196598 |
GWAS Ctlg | rs765196598 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs765196598(A;A) |
Alt | rs765196598(A;A) |
Reference | Rs765196598(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PCYT1A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.195974350G>A |
CLNSRC | |
CLNACC | RCV000412999.1, |