rs149925563
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs149925563(A;A) |
Make rs149925563(A;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 165941046 |
Gene | TTC21B, TTC21B-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs149925563 |
dbSNP (classic) | rs149925563 |
ClinGen | rs149925563 |
ebi | rs149925563 |
HLI | rs149925563 |
Exac | rs149925563 |
Gnomad | rs149925563 |
Varsome | rs149925563 |
LitVar | rs149925563 |
Map | rs149925563 |
PheGenI | rs149925563 |
Biobank | rs149925563 |
1000 genomes | rs149925563 |
hgdp | rs149925563 |
ensembl | rs149925563 |
geneview | rs149925563 |
scholar | rs149925563 |
rs149925563 | |
pharmgkb | rs149925563 |
gwascentral | rs149925563 |
openSNP | rs149925563 |
23andMe | rs149925563 |
SNPshot | rs149925563 |
SNPdbe | rs149925563 |
MSV3d | rs149925563 |
GWAS Ctlg | rs149925563 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs149925563(A;A) |
Alt | rs149925563(A;A) |
Reference | Rs149925563(T;T) |
Significance | Pathogenic |
Disease | not specified Nephronophthisis 12 |
Variation | info |
Gene | TTC21B-AS1 TTC21B |
CLNDBN | not specified Nephronophthisis 12 |
Reversed | 0 |
HGVS | NC_000002.11:g.166797556T>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000179530.1, RCV000195266.1, |