rs773734224
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs773734224(A;A) |
Make rs773734224(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 8 |
Position | 67506879 |
Gene | CPA6 |
is a | snp |
is | mentioned by |
dbSNP | rs773734224 |
dbSNP (classic) | rs773734224 |
ClinGen | rs773734224 |
ebi | rs773734224 |
HLI | rs773734224 |
Exac | rs773734224 |
Gnomad | rs773734224 |
Varsome | rs773734224 |
LitVar | rs773734224 |
Map | rs773734224 |
PheGenI | rs773734224 |
Biobank | rs773734224 |
1000 genomes | rs773734224 |
hgdp | rs773734224 |
ensembl | rs773734224 |
geneview | rs773734224 |
scholar | rs773734224 |
rs773734224 | |
pharmgkb | rs773734224 |
gwascentral | rs773734224 |
openSNP | rs773734224 |
23andMe | rs773734224 |
SNPshot | rs773734224 |
SNPdbe | rs773734224 |
MSV3d | rs773734224 |
GWAS Ctlg | rs773734224 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773734224(A;A) |
Alt | rs773734224(A;A) |
Reference | Rs773734224(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CPA6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000008.10:g.68419114G>A |
CLNSRC | |
CLNACC | RCV000171414.1, |