rs374664941
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs374664941(C;T) |
Make rs374664941(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 15644210 |
Gene | ITGA8 |
is a | snp |
is | mentioned by |
dbSNP | rs374664941 |
dbSNP (classic) | rs374664941 |
ClinGen | rs374664941 |
ebi | rs374664941 |
HLI | rs374664941 |
Exac | rs374664941 |
Gnomad | rs374664941 |
Varsome | rs374664941 |
LitVar | rs374664941 |
Map | rs374664941 |
PheGenI | rs374664941 |
Biobank | rs374664941 |
1000 genomes | rs374664941 |
hgdp | rs374664941 |
ensembl | rs374664941 |
geneview | rs374664941 |
scholar | rs374664941 |
rs374664941 | |
pharmgkb | rs374664941 |
gwascentral | rs374664941 |
openSNP | rs374664941 |
23andMe | rs374664941 |
SNPshot | rs374664941 |
SNPdbe | rs374664941 |
MSV3d | rs374664941 |
GWAS Ctlg | rs374664941 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs374664941(T;T) |
Alt | rs374664941(T;T) |
Reference | Rs374664941(C;C) |
Significance | Pathogenic |
Disease | Renal adysplasia |
Variation | info |
Gene | ITGA8 |
CLNDBN | Renal adysplasia |
Reversed | 0 |
HGVS | NC_000010.10:g.15686209C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000114395.3, |