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rs4975616

From SNPedia

Orientationplus
Stabilizedplus
Make rs4975616(A;A)
Make rs4975616(A;G)
Make rs4975616(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position1315545
is asnp
is mentioned by
dbSNPrs4975616
ebirs4975616
HLIrs4975616
Exacrs4975616
Varsomers4975616
Maprs4975616
PheGenIrs4975616
hapmaprs4975616
1000 genomesrs4975616
hgdprs4975616
ensemblrs4975616
gopubmedrs4975616
geneviewrs4975616
scholarrs4975616
googlers4975616
pharmgkbrs4975616
gwascentralrs4975616
openSNPrs4975616
23andMers4975616
23andMe allrs4975616
SNP Nexus

SNPshotrs4975616
SNPdbers4975616
MSV3drs4975616
GWAS Ctlgrs4975616
GMAF0.4118
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19654303OA-icon.png] Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study


[PMID 19836008OA-icon.png] A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.


[PMID 19955392] Role of 5p15.33 (TERT-CLPTM1L), 6p21.33 and 15q25.1 (CHRNA5-CHRNA3) variation and lung cancer risk in never-smokers.


[PMID 20445798OA-icon.png] Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.


GET Evidence
rs4975616
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.571429
summary