rs754242209
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs754242209(A;A) |
Make rs754242209(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 12 |
Position | 52515040 |
Gene | KRT5 |
is a | snp |
is | mentioned by |
dbSNP | rs754242209 |
dbSNP (classic) | rs754242209 |
ClinGen | rs754242209 |
ebi | rs754242209 |
HLI | rs754242209 |
Exac | rs754242209 |
Gnomad | rs754242209 |
Varsome | rs754242209 |
LitVar | rs754242209 |
Map | rs754242209 |
PheGenI | rs754242209 |
Biobank | rs754242209 |
1000 genomes | rs754242209 |
hgdp | rs754242209 |
ensembl | rs754242209 |
geneview | rs754242209 |
scholar | rs754242209 |
rs754242209 | |
pharmgkb | rs754242209 |
gwascentral | rs754242209 |
openSNP | rs754242209 |
23andMe | rs754242209 |
SNPshot | rs754242209 |
SNPdbe | rs754242209 |
MSV3d | rs754242209 |
GWAS Ctlg | rs754242209 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs754242209(A;A) |
Alt | rs754242209(A;A) |
Reference | Rs754242209(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | KRT5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.52908824G>A |
CLNSRC | |
CLNACC | RCV000256176.1, |