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rs10092658

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10092658(C;T)
Make rs10092658(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position129968226
GeneFAM49B
is asnp
is mentioned by
dbSNPrs10092658
ebirs10092658
HLIrs10092658
Exacrs10092658
Varsomers10092658
Maprs10092658
PheGenIrs10092658
hapmaprs10092658
1000 genomesrs10092658
hgdprs10092658
ensemblrs10092658
gopubmedrs10092658
geneviewrs10092658
scholarrs10092658
googlers10092658
pharmgkbrs10092658
gwascentralrs10092658
openSNPrs10092658
23andMers10092658
23andMe allrs10092658
SNP Nexus

SNPshotrs10092658
SNPdbers10092658
MSV3drs10092658
GWAS Ctlgrs10092658
GMAF0.03306
Max Magnitude0
? (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 0.0000060000000000000002
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Aldolase protein levels


GET Evidence
rs10092658
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0625
summary