rs397515367
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GA;GA) | 0 | common in clinvar |
Make rs397515367(-;-) |
Make rs397515367(-;GA) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 37973818 |
Gene | POLR2F, SOX10 |
is a | snp |
is | mentioned by |
dbSNP | rs397515367 |
dbSNP (classic) | rs397515367 |
ClinGen | rs397515367 |
ebi | rs397515367 |
HLI | rs397515367 |
Exac | rs397515367 |
Gnomad | rs397515367 |
Varsome | rs397515367 |
LitVar | rs397515367 |
Map | rs397515367 |
PheGenI | rs397515367 |
Biobank | rs397515367 |
1000 genomes | rs397515367 |
hgdp | rs397515367 |
ensembl | rs397515367 |
geneview | rs397515367 |
scholar | rs397515367 |
rs397515367 | |
pharmgkb | rs397515367 |
gwascentral | rs397515367 |
openSNP | rs397515367 |
23andMe | rs397515367 |
SNPshot | rs397515367 |
SNPdbe | rs397515367 |
MSV3d | rs397515367 |
GWAS Ctlg | rs397515367 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397515367(-;-) |
Alt | rs397515367(-;-) |
Reference | Rs397515367(GA;GA) |
Significance | Pathogenic |
Disease | Waardenburg syndrome type 4C |
Variation | info |
Gene | SOX10 POLR2F |
CLNDBN | Waardenburg syndrome type 4C |
Reversed | 1 |
HGVS | NC_000022.10:g.38369825_38369826delTC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000007820.3, |