rs121913130
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs121913130(A;A) |
Make rs121913130(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 4860099 |
Gene | MSX1 |
is a | snp |
is | mentioned by |
dbSNP | rs121913130 |
dbSNP (old) | rs121913130 |
ClinGen | rs121913130 |
ebi | rs121913130 |
HLI | rs121913130 |
Exac | rs121913130 |
Gnomad | rs121913130 |
Varsome | rs121913130 |
Map | rs121913130 |
PheGenI | rs121913130 |
Biobank | rs121913130 |
1000 genomes | rs121913130 |
hgdp | rs121913130 |
ensembl | rs121913130 |
gopubmed | rs121913130 |
geneview | rs121913130 |
scholar | rs121913130 |
rs121913130 | |
pharmgkb | rs121913130 |
gwascentral | rs121913130 |
openSNP | rs121913130 |
23andMe | rs121913130 |
23andMe all | rs121913130 |
SNPshot | rs121913130 |
SNPdbe | rs121913130 |
MSV3d | rs121913130 |
GWAS Ctlg | rs121913130 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913130(A;A) |
Alt | rs121913130(A;A) |
Reference | Rs121913130(T;T) |
Significance | Pathogenic |
Disease | Selective tooth agenesis 1 |
Variation | info |
Gene | MSX1 |
CLNDBN | Selective tooth agenesis 1 |
Reversed | 0 |
HGVS | NC_000004.11:g.4861826T>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000016015.22, |