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rs9033

From SNPedia

Orientationminus
Stabilizedminus
Make rs9033(C;C)
Make rs9033(C;T)
Make rs9033(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67148096
GeneB3GNT9, C16orf70
is asnp
is mentioned by
dbSNPrs9033
ebirs9033
HLIrs9033
Exacrs9033
Varsomers9033
Maprs9033
PheGenIrs9033
hapmaprs9033
1000 genomesrs9033
hgdprs9033
ensemblrs9033
gopubmedrs9033
geneviewrs9033
scholarrs9033
googlers9033
pharmgkbrs9033
gwascentralrs9033
openSNPrs9033
23andMers9033
23andMe allrs9033
SNP Nexus

SNPshotrs9033
SNPdbers9033
MSV3drs9033
GWAS Ctlgrs9033
GMAF0.4417
Max Magnitude
? (C;C) (C;T) (T;T) 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)

[PMID 18466469OA-icon.png] Genome-wide analysis of single-locus and epistasis single-nucleotide polymorphism effects on anti-cyclic citrullinated peptide as a measure of rheumatoid arthritis.

[PMID 19503744OA-icon.png] An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.

[PMID 19668596OA-icon.png] A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.