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rs897984

From SNPedia

Orientationminus
Make rs897984(A;A)
Make rs897984(A;G)
Make rs897984(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position30875322
GeneBCL7C, MIR762HG, MIR4519
is asnp
is mentioned by
dbSNPrs897984
ebirs897984
HLIrs897984
Exacrs897984
Varsomers897984
Maprs897984
PheGenIrs897984
hapmaprs897984
1000 genomesrs897984
hgdprs897984
ensemblrs897984
gopubmedrs897984
geneviewrs897984
scholarrs897984
googlers897984
pharmgkbrs897984
gwascentralrs897984
openSNPrs897984
23andMers897984
23andMe allrs897984
SNP Nexus

SNPshotrs897984
SNPdbers897984
MSV3drs897984
GWAS Ctlgrs897984
Max Magnitude

[PMID 26670097] Genetic Variants in MicroRNAs and their Binding Sites are Associated with the Risk of Parkinson Disease