Have questions? Visit https://www.reddit.com/r/SNPedia

rs1368474

From SNPedia

Orientationplus
Stabilizedplus
Make rs1368474(C;C)
Make rs1368474(C;T)
Make rs1368474(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position14259776
is asnp
is mentioned by
dbSNPrs1368474
ebirs1368474
HLIrs1368474
Exacrs1368474
Varsomers1368474
Maprs1368474
PheGenIrs1368474
hapmaprs1368474
1000 genomesrs1368474
hgdprs1368474
ensemblrs1368474
gopubmedrs1368474
geneviewrs1368474
scholarrs1368474
googlers1368474
pharmgkbrs1368474
gwascentralrs1368474
openSNPrs1368474
23andMers1368474
23andMe allrs1368474
SNP Nexus

SNPshotrs1368474
SNPdbers1368474
MSV3drs1368474
GWAS Ctlgrs1368474
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25227856] Exploratory investigation of genetic associations with Basal cell carcinoma risk: genome-wide association study in jeju island, Korea