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rs7763881

From SNPedia

Orientationplus
Stabilizedplus
Make rs7763881(A;A)
Make rs7763881(A;C)
Make rs7763881(C;C)
ReferenceGRCh38 38.1/142
Chromosome6
Position8653014
GeneHULC, LOC100506207
is asnp
is mentioned by
dbSNPrs7763881
ebirs7763881
HLIrs7763881
Exacrs7763881
Varsomers7763881
Maprs7763881
PheGenIrs7763881
hapmaprs7763881
1000 genomesrs7763881
hgdprs7763881
ensemblrs7763881
gopubmedrs7763881
geneviewrs7763881
scholarrs7763881
googlers7763881
pharmgkbrs7763881
gwascentralrs7763881
openSNPrs7763881
23andMers7763881
23andMe allrs7763881
SNP Nexus

SNPshotrs7763881
SNPdbers7763881
MSV3drs7763881
GWAS Ctlgrs7763881
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 25874495] Long noncoding RNAs POLR2E rs3787016 C/T and HULC rs7763881 A/C polymorphisms are associated with decreased risk of esophageal cancer