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rs6472866

From SNPedia

Orientationplus
Stabilizedplus
Make rs6472866(C;C)
Make rs6472866(C;T)
Make rs6472866(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position74600899
GeneRNF41
is asnp
is mentioned by
dbSNPrs6472866
ebirs6472866
HLIrs6472866
Exacrs6472866
Varsomers6472866
Maprs6472866
PheGenIrs6472866
hapmaprs6472866
1000 genomesrs6472866
hgdprs6472866
ensemblrs6472866
gopubmedrs6472866
geneviewrs6472866
scholarrs6472866
googlers6472866
pharmgkbrs6472866
gwascentralrs6472866
openSNPrs6472866
23andMers6472866
23andMe allrs6472866
SNP Nexus

SNPshotrs6472866
SNPdbers6472866
MSV3drs6472866
GWAS Ctlgrs6472866
GMAF0.4871
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18464913OA-icon.png]
Trait Protein quantitative trait loci
Title A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
Risk Allele
P-val 7.9999999999999996E-7
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Myoglobin (MB) protein levels


GET Evidence
rs6472866
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484127
summary