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rs846111

From SNPedia

Orientationminus
Stabilizedplus
Make rs846111(C;C)
Make rs846111(C;G)
Make rs846111(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position6219310
GeneRNF207
is asnp
is mentioned by
dbSNPrs846111
ebirs846111
HLIrs846111
Exacrs846111
Varsomers846111
Maprs846111
PheGenIrs846111
hapmaprs846111
1000 genomesrs846111
hgdprs846111
ensemblrs846111
gopubmedrs846111
geneviewrs846111
scholarrs846111
googlers846111
pharmgkbrs846111
gwascentralrs846111
openSNPrs846111
23andMers846111
23andMe allrs846111
SNP Nexus

SNPshotrs846111
SNPdbers846111
MSV3drs846111
GWAS Ctlgrs846111
GMAF0.174
Max Magnitude
? (C;C) (C;G) (G;G) 28
23andMe blog Influences QT interval
GWAS snp
PMID [PMID 19305408OA-icon.png]
Trait QT interval
Title Common variants at ten loci influence QT interval duation in the QTGEN Study
Risk Allele C
P-val 1E-16
Odds Ratio 1.75 [1.41-2.09] msec increase
GWAS snp
PMID [PMID 19305409OA-icon.png]
Trait QT interval
Title Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Risk Allele C
P-val 4E-16
Odds Ratio 1.49 [1.00-1.98] ms increase




GET Evidence
RNF207-G603A
aa_change Gly603Ala
aa_change_short G603A
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.198737
summary