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rs112310158

From SNPedia

Orientationplus
Stabilizedplus
Make rs112310158(A;A)
Make rs112310158(A;G)
Make rs112310158(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position55170550
GeneCDC20B, MIR449A, MIR449B
is asnp
is mentioned by
dbSNPrs112310158
dbSNP (old)rs112310158
ClinGenrs112310158
ebirs112310158
HLIrs112310158
Exacrs112310158
Gnomadrs112310158
Varsomers112310158
Maprs112310158
PheGenIrs112310158
Biobankrs112310158
1000 genomesrs112310158
hgdprs112310158
ensemblrs112310158
gopubmedrs112310158
geneviewrs112310158
scholarrs112310158
googlers112310158
pharmgkbrs112310158
gwascentralrs112310158
openSNPrs112310158
23andMers112310158
23andMe allrs112310158
SNP Nexus

SNPshotrs112310158
SNPdbers112310158
MSV3drs112310158
GWAS Ctlgrs112310158
Max Magnitude

[PMID 26722545OA-icon.png] Hsa-miR-449a genetic variant is associated with risk of gastric cancer in a Chinese population.