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rs6715866

From SNPedia

Orientationplus
Make rs6715866(C;C)
Make rs6715866(C;T)
Make rs6715866(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position38760475
is asnp
is mentioned by
dbSNPrs6715866
ebirs6715866
HLIrs6715866
Exacrs6715866
Varsomers6715866
Maprs6715866
PheGenIrs6715866
hapmaprs6715866
1000 genomesrs6715866
hgdprs6715866
ensemblrs6715866
gopubmedrs6715866
geneviewrs6715866
scholarrs6715866
googlers6715866
pharmgkbrs6715866
gwascentralrs6715866
openSNPrs6715866
23andMers6715866
23andMe allrs6715866
SNP Nexus

SNPshotrs6715866
SNPdbers6715866
MSV3drs6715866
GWAS Ctlgrs6715866
Max Magnitude
? (C;C) (C;T) (T;T) 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 (as oriented in SNPedia and dbSNP).