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rs6750998

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs6750998(A;A)
Make rs6750998(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position88583424
GeneEIF2AK3
is asnp
is mentioned by
dbSNPrs6750998
ebirs6750998
HLIrs6750998
Exacrs6750998
Varsomers6750998
Maprs6750998
PheGenIrs6750998
hapmaprs6750998
1000 genomesrs6750998
hgdprs6750998
ensemblrs6750998
gopubmedrs6750998
geneviewrs6750998
scholarrs6750998
googlers6750998
pharmgkbrs6750998
gwascentralrs6750998
openSNPrs6750998
23andMers6750998
23andMe allrs6750998
SNP Nexus

SNPshotrs6750998
SNPdbers6750998
MSV3drs6750998
GWAS Ctlgrs6750998
Max Magnitude0
? (A;A) (A;T) (T;T) 28

[PMID 24985580] Common variants in PERK, JNK, BIP and XBP1 genes are associated with the risk of prediabetes or diabetes-related phenotypes in a Chinese population


ClinVar
Risk rs6750998(A;A)
Alt rs6750998(A;A)
Reference rs6750998(T;T)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene EIF2AK3
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.88882942T>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000116966.2,