rs387906841
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs387906841(A;T) |
Make rs387906841(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31117440 |
Gene | CDSN, PSORS1C1 |
is a | snp |
is | mentioned by |
dbSNP | rs387906841 |
dbSNP (classic) | rs387906841 |
ClinGen | rs387906841 |
ebi | rs387906841 |
HLI | rs387906841 |
Exac | rs387906841 |
Gnomad | rs387906841 |
Varsome | rs387906841 |
LitVar | rs387906841 |
Map | rs387906841 |
PheGenI | rs387906841 |
Biobank | rs387906841 |
1000 genomes | rs387906841 |
hgdp | rs387906841 |
ensembl | rs387906841 |
geneview | rs387906841 |
scholar | rs387906841 |
rs387906841 | |
pharmgkb | rs387906841 |
gwascentral | rs387906841 |
openSNP | rs387906841 |
23andMe | rs387906841 |
SNPshot | rs387906841 |
SNPdbe | rs387906841 |
MSV3d | rs387906841 |
GWAS Ctlg | rs387906841 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906841(T;T) |
Alt | rs387906841(T;T) |
Reference | Rs387906841(A;A) |
Significance | Pathogenic |
Disease | Peeling skin syndrome |
Variation | info |
Gene | CDSN PSORS1C1 |
CLNDBN | Peeling skin syndrome |
Reversed | 1 |
HGVS | NC_000006.11:g.31085217T>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023198.3, |