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rs2236316

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2236316(C;C)
Make rs2236316(C;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position50757699
GeneNIN
is asnp
is mentioned by
dbSNPrs2236316
ebirs2236316
HLIrs2236316
Exacrs2236316
Varsomers2236316
Maprs2236316
PheGenIrs2236316
hapmaprs2236316
1000 genomesrs2236316
hgdprs2236316
ensemblrs2236316
gopubmedrs2236316
geneviewrs2236316
scholarrs2236316
googlers2236316
pharmgkbrs2236316
gwascentralrs2236316
openSNPrs2236316
23andMers2236316
23andMe allrs2236316
SNP Nexus

SNPshotrs2236316
SNPdbers2236316
MSV3drs2236316
GWAS Ctlgrs2236316
GMAF0.1841
Max Magnitude0
? (C;C) (C;G) (G;G) 28
Venter snp
Source plos
Gene NIN
allele C
frequency 0.325
sift TOLERATED
HuRef 1103649060175
Disease Association Antibodies against NIN are present in sera from patients with autoimmune diseases that developed autoantibodies against centrosomal proteins.



Neighborrs2073347
Distance628


GET Evidence
NIN-P1111A
aa_change Pro1111Ala
aa_change_short P1111A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.198922
summary



ClinVar
Risk rs2236316(C;C)
Alt rs2236316(C;C)
Reference rs2236316(G;G)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene NIN
CLNDBN not specified
Reversed 0
HGVS NC_000014.8:g.51224417G>C
CLNSRC ClinVar University of Chicago
CLNACC RCV000117803.2,