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rs1494961

From SNPedia

Orientationplus
Stabilizedplus
Make rs1494961(C;C)
Make rs1494961(C;T)
Make rs1494961(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position83453327
GeneHELQ
is asnp
is mentioned by
dbSNPrs1494961
ebirs1494961
HLIrs1494961
Exacrs1494961
Varsomers1494961
Maprs1494961
PheGenIrs1494961
hapmaprs1494961
1000 genomesrs1494961
hgdprs1494961
ensemblrs1494961
gopubmedrs1494961
geneviewrs1494961
scholarrs1494961
googlers1494961
pharmgkbrs1494961
gwascentralrs1494961
openSNPrs1494961
23andMers1494961
23andMe allrs1494961
SNP Nexus

SNPshotrs1494961
SNPdbers1494961
MSV3drs1494961
GWAS Ctlgrs1494961
GMAF0.3737
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21437268OA-icon.png] A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium


GET Evidence
HELQ-V306I
aa_change Val306Ile
aa_change_short V306I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.592303
summary



[PMID 23430454] Genetic variants at 4q21, 4q23 and 12q24 are associated with esophageal squamous cell carcinoma risk in a Chinese population