rs370243877
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs370243877(A;T) |
Make rs370243877(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 47941773 |
Gene | PNPO, SP2-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs370243877 |
dbSNP (classic) | rs370243877 |
ClinGen | rs370243877 |
ebi | rs370243877 |
HLI | rs370243877 |
Exac | rs370243877 |
Gnomad | rs370243877 |
Varsome | rs370243877 |
LitVar | rs370243877 |
Map | rs370243877 |
PheGenI | rs370243877 |
Biobank | rs370243877 |
1000 genomes | rs370243877 |
hgdp | rs370243877 |
ensembl | rs370243877 |
geneview | rs370243877 |
scholar | rs370243877 |
rs370243877 | |
pharmgkb | rs370243877 |
gwascentral | rs370243877 |
openSNP | rs370243877 |
23andMe | rs370243877 |
SNPshot | rs370243877 |
SNPdbe | rs370243877 |
MSV3d | rs370243877 |
GWAS Ctlg | rs370243877 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs370243877(T;T) |
Alt | rs370243877(T;T) |
Reference | Rs370243877(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | LOC100506325 SP2-AS1 PNPO |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.46019139A>T |
CLNSRC | |
CLNACC | RCV000188506.3, |