rs876657660
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs876657660(C;C) |
Make rs876657660(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 37983384 |
Gene | POLR2F, SOX10 |
is a | snp |
is | mentioned by |
dbSNP | rs876657660 |
dbSNP (classic) | rs876657660 |
ClinGen | rs876657660 |
ebi | rs876657660 |
HLI | rs876657660 |
Exac | rs876657660 |
Gnomad | rs876657660 |
Varsome | rs876657660 |
LitVar | rs876657660 |
Map | rs876657660 |
PheGenI | rs876657660 |
Biobank | rs876657660 |
1000 genomes | rs876657660 |
hgdp | rs876657660 |
ensembl | rs876657660 |
geneview | rs876657660 |
scholar | rs876657660 |
rs876657660 | |
pharmgkb | rs876657660 |
gwascentral | rs876657660 |
openSNP | rs876657660 |
23andMe | rs876657660 |
SNPshot | rs876657660 |
SNPdbe | rs876657660 |
MSV3d | rs876657660 |
GWAS Ctlg | rs876657660 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876657660(C;C) |
Alt | rs876657660(C;C) |
Reference | Rs876657660(T;T) |
Significance | Probable-Pathogenic |
Disease | Waardenburg syndrome |
Variation | info |
Gene | SOX10 POLR2F |
CLNDBN | Waardenburg syndrome |
Reversed | 1 |
HGVS | NC_000022.10:g.38379391A>G |
CLNSRC | |
CLNACC | RCV000215786.1, |