rs766090540
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs766090540(A;A) |
Make rs766090540(A;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 43430098 |
Gene | SZT2 |
is a | snp |
is | mentioned by |
dbSNP | rs766090540 |
dbSNP (classic) | rs766090540 |
ClinGen | rs766090540 |
ebi | rs766090540 |
HLI | rs766090540 |
Exac | rs766090540 |
Gnomad | rs766090540 |
Varsome | rs766090540 |
LitVar | rs766090540 |
Map | rs766090540 |
PheGenI | rs766090540 |
Biobank | rs766090540 |
1000 genomes | rs766090540 |
hgdp | rs766090540 |
ensembl | rs766090540 |
geneview | rs766090540 |
scholar | rs766090540 |
rs766090540 | |
pharmgkb | rs766090540 |
gwascentral | rs766090540 |
openSNP | rs766090540 |
23andMe | rs766090540 |
SNPshot | rs766090540 |
SNPdbe | rs766090540 |
MSV3d | rs766090540 |
GWAS Ctlg | rs766090540 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs766090540(A;A) rs766090540(T;T) |
Alt | rs766090540(A;A) rs766090540(T;T) |
Reference | Rs766090540(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SZT2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43895769C>T |
CLNSRC | |
CLNACC | RCV000363038.1, |