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rs76481776

From SNPedia

Orientationplus
Stabilizedplus
Make rs76481776(C;C)
Make rs76481776(C;T)
Make rs76481776(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position129770387
GeneMIR182
is asnp
is mentioned by
dbSNPrs76481776
ebirs76481776
HLIrs76481776
Exacrs76481776
Varsomers76481776
Maprs76481776
PheGenIrs76481776
hapmaprs76481776
1000 genomesrs76481776
hgdprs76481776
ensemblrs76481776
gopubmedrs76481776
geneviewrs76481776
scholarrs76481776
googlers76481776
pharmgkbrs76481776
gwascentralrs76481776
openSNPrs76481776
23andMers76481776
23andMe allrs76481776
SNP Nexus

SNPshotrs76481776
SNPdbers76481776
MSV3drs76481776
GWAS Ctlgrs76481776
Max Magnitude

[PMID 24801147] Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182