rs121909488
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121909488(G;T) |
Make rs121909488(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 126690862 |
Gene | LMX1B |
is a | snp |
is | mentioned by |
dbSNP | rs121909488 |
dbSNP (classic) | rs121909488 |
ClinGen | rs121909488 |
ebi | rs121909488 |
HLI | rs121909488 |
Exac | rs121909488 |
Gnomad | rs121909488 |
Varsome | rs121909488 |
LitVar | rs121909488 |
Map | rs121909488 |
PheGenI | rs121909488 |
Biobank | rs121909488 |
1000 genomes | rs121909488 |
hgdp | rs121909488 |
ensembl | rs121909488 |
geneview | rs121909488 |
scholar | rs121909488 |
rs121909488 | |
pharmgkb | rs121909488 |
gwascentral | rs121909488 |
openSNP | rs121909488 |
23andMe | rs121909488 |
SNPshot | rs121909488 |
SNPdbe | rs121909488 |
MSV3d | rs121909488 |
GWAS Ctlg | rs121909488 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909488(T;T) |
Alt | rs121909488(T;T) |
Reference | Rs121909488(G;G) |
Significance | Pathogenic |
Disease | Nail-patella syndrome |
Variation | info |
Gene | LMX1B |
CLNDBN | Nail-patella syndrome |
Reversed | 0 |
HGVS | NC_000009.11:g.129453141G>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000007418.2, |