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rs9322817

From SNPedia

Orientationplus
Stabilizedplus
Make rs9322817(A;A)
Make rs9322817(A;C)
Make rs9322817(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position104784358
GeneHACE1
is asnp
is mentioned by
dbSNPrs9322817
ebirs9322817
HLIrs9322817
Exacrs9322817
Varsomers9322817
Maprs9322817
PheGenIrs9322817
hapmaprs9322817
1000 genomesrs9322817
hgdprs9322817
ensemblrs9322817
gopubmedrs9322817
geneviewrs9322817
scholarrs9322817
googlers9322817
pharmgkbrs9322817
gwascentralrs9322817
openSNPrs9322817
23andMers9322817
23andMe allrs9322817
SNP Nexus

SNPshotrs9322817
SNPdbers9322817
MSV3drs9322817
GWAS Ctlgrs9322817
GMAF0.3907
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs9322817
PubMedID [PMID 17903292OA-icon.png]
Condition Thyroid stimulating hormone
Gene HACE1
Risk Allele
pValue 7.00E-006
OR NA
95% CI



GET Evidence
rs9322817
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.398887
summary