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rs6930337

From SNPedia

Orientationplus
Stabilizedplus
Make rs6930337(C;C)
Make rs6930337(C;T)
Make rs6930337(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position148466870
GeneSASH1
is asnp
is mentioned by
dbSNPrs6930337
ebirs6930337
HLIrs6930337
Exacrs6930337
Varsomers6930337
Maprs6930337
PheGenIrs6930337
hapmaprs6930337
1000 genomesrs6930337
hgdprs6930337
ensemblrs6930337
gopubmedrs6930337
geneviewrs6930337
scholarrs6930337
googlers6930337
pharmgkbrs6930337
gwascentralrs6930337
openSNPrs6930337
23andMers6930337
23andMe allrs6930337
SNP Nexus

SNPshotrs6930337
SNPdbers6930337
MSV3drs6930337
GWAS Ctlgrs6930337
GMAF0.1309
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 9.9999999999999995E-7
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Insulin (INS) protein levels


GET Evidence
rs6930337
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary