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rs7784168

From SNPedia

Orientationplus
Stabilizedplus
Make rs7784168(C;C)
Make rs7784168(C;T)
Make rs7784168(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position124851984
GenePOT1
is asnp
is mentioned by
dbSNPrs7784168
ebirs7784168
HLIrs7784168
Exacrs7784168
Varsomers7784168
Maprs7784168
PheGenIrs7784168
hapmaprs7784168
1000 genomesrs7784168
hgdprs7784168
ensemblrs7784168
gopubmedrs7784168
geneviewrs7784168
scholarrs7784168
googlers7784168
pharmgkbrs7784168
gwascentralrs7784168
openSNPrs7784168
23andMers7784168
23andMe allrs7784168
SNP Nexus

SNPshotrs7784168
SNPdbers7784168
MSV3drs7784168
GWAS Ctlgrs7784168
GMAF0.281
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23907815] Prognostic impact of telomere maintenance gene polymorphisms in hepatocellular carcinoma patients with chronic Hepatitis B