rs2245639
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2245639(A;A) |
Make rs2245639(A;C) |
Make rs2245639(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 19590865 |
is a | snp |
is | mentioned by |
dbSNP | rs2245639 |
dbSNP (classic) | rs2245639 |
ClinGen | rs2245639 |
ebi | rs2245639 |
HLI | rs2245639 |
Exac | rs2245639 |
Gnomad | rs2245639 |
Varsome | rs2245639 |
LitVar | rs2245639 |
Map | rs2245639 |
PheGenI | rs2245639 |
Biobank | rs2245639 |
1000 genomes | rs2245639 |
hgdp | rs2245639 |
ensembl | rs2245639 |
geneview | rs2245639 |
scholar | rs2245639 |
rs2245639 | |
pharmgkb | rs2245639 |
gwascentral | rs2245639 |
openSNP | rs2245639 |
23andMe | rs2245639 |
SNPshot | rs2245639 |
SNPdbe | rs2245639 |
MSV3d | rs2245639 |
GWAS Ctlg | rs2245639 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 25855245] Case of Sjögren-Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis