rs1368474
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1368474(C;C) |
Make rs1368474(C;T) |
Make rs1368474(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 14259776 |
is a | snp |
is | mentioned by |
dbSNP | rs1368474 |
dbSNP (classic) | rs1368474 |
ClinGen | rs1368474 |
ebi | rs1368474 |
HLI | rs1368474 |
Exac | rs1368474 |
Gnomad | rs1368474 |
Varsome | rs1368474 |
LitVar | rs1368474 |
Map | rs1368474 |
PheGenI | rs1368474 |
Biobank | rs1368474 |
1000 genomes | rs1368474 |
hgdp | rs1368474 |
ensembl | rs1368474 |
geneview | rs1368474 |
scholar | rs1368474 |
rs1368474 | |
pharmgkb | rs1368474 |
gwascentral | rs1368474 |
openSNP | rs1368474 |
23andMe | rs1368474 |
SNPshot | rs1368474 |
SNPdbe | rs1368474 |
MSV3d | rs1368474 |
GWAS Ctlg | rs1368474 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25227856] Exploratory investigation of genetic associations with Basal cell carcinoma risk: genome-wide association study in jeju island, Korea