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rs56489998

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs56489998(C;C)
Make rs56489998(C;T)
Make rs56489998(T;T)
ReferenceGRCh37.p5 37.3/135
ChromosomeMT
Position663
GeneMT-RNR1
is asnp
is mentioned by
dbSNPrs56489998
ebirs56489998
HLIrs56489998
Exacrs56489998
Varsomers56489998
Maprs56489998
PheGenIrs56489998
hapmaprs56489998
1000 genomesrs56489998
hgdprs56489998
ensemblrs56489998
gopubmedrs56489998
geneviewrs56489998
scholarrs56489998
googlers56489998
pharmgkbrs56489998
gwascentralrs56489998
openSNPrs56489998
23andMers56489998
23andMe allrs56489998
SNP Nexus

SNPshotrs56489998
SNPdbers56489998
MSV3drs56489998
GWAS Ctlgrs56489998
Merged fromRs3937039
GMAF0.07951
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19458495OA-icon.png] Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.