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rs16835244

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16835244(G;T)
Make rs16835244(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position33096815
GeneADC
is asnp
is mentioned by
dbSNPrs16835244
ebirs16835244
HLIrs16835244
Exacrs16835244
Varsomers16835244
Maprs16835244
PheGenIrs16835244
hapmaprs16835244
1000 genomesrs16835244
hgdprs16835244
ensemblrs16835244
gopubmedrs16835244
geneviewrs16835244
scholarrs16835244
googlers16835244
pharmgkbrs16835244
gwascentralrs16835244
openSNPrs16835244
23andMers16835244
23andMe allrs16835244
SNP Nexus

SNPshotrs16835244
SNPdbers16835244
MSV3drs16835244
GWAS Ctlgrs16835244
GMAF0.04408
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 20147969] Non-synonymous single-nucleotide polymorphisms associated with blood pressure and hypertension


GET Evidence
ADC-A288S
aa_change Ala288Ser
aa_change_short A288S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.00102249
summary



ClinVar
Risk rs16835244(T;T)
Alt rs16835244(T;T)
Reference Rs16835244(G;G)
Significance Untested
Disease not provided
Variation info
Gene AZIN2 ADC
CLNDBN not provided
Reversed 0
HGVS NC_000001.11:g.33096815G>T
CLNSRC ClinVar Emory University
CLNACC RCV000082331.1,