rs757674160
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs757674160(A;G) |
Make rs757674160(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 56836704 |
Gene | NUP93 |
is a | snp |
is | mentioned by |
dbSNP | rs757674160 |
dbSNP (classic) | rs757674160 |
ClinGen | rs757674160 |
ebi | rs757674160 |
HLI | rs757674160 |
Exac | rs757674160 |
Gnomad | rs757674160 |
Varsome | rs757674160 |
LitVar | rs757674160 |
Map | rs757674160 |
PheGenI | rs757674160 |
Biobank | rs757674160 |
1000 genomes | rs757674160 |
hgdp | rs757674160 |
ensembl | rs757674160 |
geneview | rs757674160 |
scholar | rs757674160 |
rs757674160 | |
pharmgkb | rs757674160 |
gwascentral | rs757674160 |
openSNP | rs757674160 |
23andMe | rs757674160 |
SNPshot | rs757674160 |
SNPdbe | rs757674160 |
MSV3d | rs757674160 |
GWAS Ctlg | rs757674160 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757674160(G;G) |
Alt | rs757674160(G;G) |
Reference | Rs757674160(A;A) |
Significance | Pathogenic |
Disease | Nephrotic syndrome |
Variation | info |
Gene | NUP93 |
CLNDBN | Nephrotic syndrome, type 12 |
Reversed | 0 |
HGVS | NC_000016.9:g.56870616A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000210657.1, |