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rs9939768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs9939768(C;C)
Make rs9939768(C;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position67185204
GeneEXOC3L, KIAA0895L
is asnp
is mentioned by
dbSNPrs9939768
ebirs9939768
HLIrs9939768
Exacrs9939768
Varsomers9939768
Maprs9939768
PheGenIrs9939768
hapmaprs9939768
1000 genomesrs9939768
hgdprs9939768
ensemblrs9939768
gopubmedrs9939768
geneviewrs9939768
scholarrs9939768
googlers9939768
pharmgkbrs9939768
gwascentralrs9939768
openSNPrs9939768
23andMers9939768
23andMe allrs9939768
SNP Nexus

SNPshotrs9939768
SNPdbers9939768
MSV3drs9939768
GWAS Ctlgrs9939768
GMAF0.1492
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 19854717OA-icon.png] The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD)


GET Evidence
EXOC3L-Q561E
aa_change Gln561Glu
aa_change_short Q561E
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.187024
summary