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rs7577642

From SNPedia

Orientationplus
Stabilizedplus
Make rs7577642(C;C)
Make rs7577642(C;T)
Make rs7577642(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position85472627
is asnp
is mentioned by
dbSNPrs7577642
ebirs7577642
HLIrs7577642
Exacrs7577642
Varsomers7577642
Maprs7577642
PheGenIrs7577642
hapmaprs7577642
1000 genomesrs7577642
hgdprs7577642
ensemblrs7577642
gopubmedrs7577642
geneviewrs7577642
scholarrs7577642
googlers7577642
pharmgkbrs7577642
gwascentralrs7577642
openSNPrs7577642
23andMers7577642
23andMe allrs7577642
SNP Nexus

SNPshotrs7577642
SNPdbers7577642
MSV3drs7577642
GWAS Ctlgrs7577642
GMAF0.2493
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 0.0000069999999999999999
Odds Ratio NR NR

[PMID 18464913OA-icon.png] soluble IL6R (sIL-6R) protein levels


GET Evidence
rs7577642
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.679688
summary