rs552219028
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs552219028(A;C) |
Make rs552219028(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 122923143 |
Gene | NUDT6, SPATA5 |
is a | snp |
is | mentioned by |
dbSNP | rs552219028 |
dbSNP (classic) | rs552219028 |
ClinGen | rs552219028 |
ebi | rs552219028 |
HLI | rs552219028 |
Exac | rs552219028 |
Gnomad | rs552219028 |
Varsome | rs552219028 |
LitVar | rs552219028 |
Map | rs552219028 |
PheGenI | rs552219028 |
Biobank | rs552219028 |
1000 genomes | rs552219028 |
hgdp | rs552219028 |
ensembl | rs552219028 |
geneview | rs552219028 |
scholar | rs552219028 |
rs552219028 | |
pharmgkb | rs552219028 |
gwascentral | rs552219028 |
openSNP | rs552219028 |
23andMe | rs552219028 |
SNPshot | rs552219028 |
SNPdbe | rs552219028 |
MSV3d | rs552219028 |
GWAS Ctlg | rs552219028 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs552219028(C;C) rs552219028(G;G) rs552219028(T;T) |
Alt | rs552219028(C;C) rs552219028(G;G) rs552219028(T;T) |
Reference | Rs552219028(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | NUDT6 SPATA5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.123844298A>C |
CLNSRC | |
CLNACC | RCV000185657.2, |