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rs16876385

From SNPedia

Orientationplus
Make rs16876385(C;C)
Make rs16876385(C;G)
Make rs16876385(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position85625246
GeneSYNCRIP
is asnp
is mentioned by
dbSNPrs16876385
ebirs16876385
HLIrs16876385
Exacrs16876385
Varsomers16876385
Maprs16876385
PheGenIrs16876385
hapmaprs16876385
1000 genomesrs16876385
hgdprs16876385
ensemblrs16876385
gopubmedrs16876385
geneviewrs16876385
scholarrs16876385
googlers16876385
pharmgkbrs16876385
gwascentralrs16876385
openSNPrs16876385
23andMers16876385
23andMe allrs16876385
SNP Nexus

SNPshotrs16876385
SNPdbers16876385
MSV3drs16876385
GWAS Ctlgrs16876385
Max Magnitude
? (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.