rs16876385
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16876385(C;C) |
Make rs16876385(C;G) |
Make rs16876385(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 85625246 |
Gene | SYNCRIP |
is a | snp |
is | mentioned by |
dbSNP | rs16876385 |
dbSNP (classic) | rs16876385 |
ClinGen | rs16876385 |
ebi | rs16876385 |
HLI | rs16876385 |
Exac | rs16876385 |
Gnomad | rs16876385 |
Varsome | rs16876385 |
LitVar | rs16876385 |
Map | rs16876385 |
PheGenI | rs16876385 |
Biobank | rs16876385 |
1000 genomes | rs16876385 |
hgdp | rs16876385 |
ensembl | rs16876385 |
geneview | rs16876385 |
scholar | rs16876385 |
rs16876385 | |
pharmgkb | rs16876385 |
gwascentral | rs16876385 |
openSNP | rs16876385 |
23andMe | rs16876385 |
SNPshot | rs16876385 |
SNPdbe | rs16876385 |
MSV3d | rs16876385 |
GWAS Ctlg | rs16876385 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 26162562] Polymorphisms in alternative splicing associated genes are associated with lung cancer risk in a Chinese population. This study found risk associated with the C allele.