rs121909117
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121909117(C;T) |
Make rs121909117(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 37978094 |
Gene | POLR2F, SOX10 |
is a | snp |
is | mentioned by |
dbSNP | rs121909117 |
dbSNP (classic) | rs121909117 |
ClinGen | rs121909117 |
ebi | rs121909117 |
HLI | rs121909117 |
Exac | rs121909117 |
Gnomad | rs121909117 |
Varsome | rs121909117 |
LitVar | rs121909117 |
Map | rs121909117 |
PheGenI | rs121909117 |
Biobank | rs121909117 |
1000 genomes | rs121909117 |
hgdp | rs121909117 |
ensembl | rs121909117 |
geneview | rs121909117 |
scholar | rs121909117 |
rs121909117 | |
pharmgkb | rs121909117 |
gwascentral | rs121909117 |
openSNP | rs121909117 |
23andMe | rs121909117 |
SNPshot | rs121909117 |
SNPdbe | rs121909117 |
MSV3d | rs121909117 |
GWAS Ctlg | rs121909117 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909117(T;T) |
Alt | rs121909117(T;T) |
Reference | Rs121909117(C;C) |
Significance | Pathogenic |
Disease | Waardenburg syndrome type 4C |
Variation | info |
Gene | SOX10 POLR2F |
CLNDBN | Waardenburg syndrome type 4C |
Reversed | 1 |
HGVS | NC_000022.10:g.38374101G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000007833.6, |