rs267607475
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(ATCGCCACCTACCGCAAGCTGCTGGAG;ATCGCCACCTACCGCAAGCTGCTGGAG) | 0 | common in clinvar |
Make rs267607475(-;-) |
Make rs267607475(-;ATCGCCACCTACCGCAAGCTGCTGGAG) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 52469684 |
Gene | KRT6C |
is a | snp |
is | mentioned by |
dbSNP | rs267607475 |
dbSNP (classic) | rs267607475 |
ClinGen | rs267607475 |
ebi | rs267607475 |
HLI | rs267607475 |
Exac | rs267607475 |
Gnomad | rs267607475 |
Varsome | rs267607475 |
LitVar | rs267607475 |
Map | rs267607475 |
PheGenI | rs267607475 |
Biobank | rs267607475 |
1000 genomes | rs267607475 |
hgdp | rs267607475 |
ensembl | rs267607475 |
geneview | rs267607475 |
scholar | rs267607475 |
rs267607475 | |
pharmgkb | rs267607475 |
gwascentral | rs267607475 |
openSNP | rs267607475 |
23andMe | rs267607475 |
SNPshot | rs267607475 |
SNPdbe | rs267607475 |
MSV3d | rs267607475 |
GWAS Ctlg | rs267607475 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267607475(-;-) |
Alt | rs267607475(-;-) |
Reference | Rs267607475(ATCGCCACCTACCGCAAGCTGCTGGAG;ATCGCCACCTACCGCAAGCTGCTGGAG) |
Significance | Pathogenic |
Disease | not provided Palmoplantar keratoderma |
Variation | info |
Gene | KRT6C |
CLNDBN | not provided Palmoplantar keratoderma, nonepidermolytic, focal |
Reversed | 1 |
HGVS | NC_000012.11:g.52863468_52863494del27 |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000057499.1, RCV000114417.2, |