rs397515371
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs397515371(-;-) |
Make rs397515371(-;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 37974099 |
Gene | POLR2F, SOX10 |
is a | snp |
is | mentioned by |
dbSNP | rs397515371 |
dbSNP (classic) | rs397515371 |
ClinGen | rs397515371 |
ebi | rs397515371 |
HLI | rs397515371 |
Exac | rs397515371 |
Gnomad | rs397515371 |
Varsome | rs397515371 |
LitVar | rs397515371 |
Map | rs397515371 |
PheGenI | rs397515371 |
Biobank | rs397515371 |
1000 genomes | rs397515371 |
hgdp | rs397515371 |
ensembl | rs397515371 |
geneview | rs397515371 |
scholar | rs397515371 |
rs397515371 | |
pharmgkb | rs397515371 |
gwascentral | rs397515371 |
openSNP | rs397515371 |
23andMe | rs397515371 |
SNPshot | rs397515371 |
SNPdbe | rs397515371 |
MSV3d | rs397515371 |
GWAS Ctlg | rs397515371 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397515371(-;-) |
Alt | rs397515371(-;-) |
Reference | Rs397515371(G;G) |
Significance | Pathogenic |
Disease | Peripheral demyelinating neuropathy |
Variation | info |
Gene | SOX10 POLR2F |
CLNDBN | Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease |
Reversed | 1 |
HGVS | NC_000022.10:g.38370106delC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000007836.5, |