rs2395
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2395(A;A) |
Make rs2395(A;G) |
Make rs2395(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 45303351 |
Gene | MARK4 |
is a | snp |
is | mentioned by |
dbSNP | rs2395 |
dbSNP (classic) | rs2395 |
ClinGen | rs2395 |
ebi | rs2395 |
HLI | rs2395 |
Exac | rs2395 |
Gnomad | rs2395 |
Varsome | rs2395 |
LitVar | rs2395 |
Map | rs2395 |
PheGenI | rs2395 |
Biobank | rs2395 |
1000 genomes | rs2395 |
hgdp | rs2395 |
ensembl | rs2395 |
geneview | rs2395 |
scholar | rs2395 |
rs2395 | |
pharmgkb | rs2395 |
gwascentral | rs2395 |
openSNP | rs2395 |
23andMe | rs2395 |
SNPshot | rs2395 |
SNPdbe | rs2395 |
MSV3d | rs2395 |
GWAS Ctlg | rs2395 |
GMAF | 0.41 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22506312] Investigation of two Wnt signalling pathway single nucleotide polymorphisms in a breast cancer-affected Australian population