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rs2086310

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2086310(C;G)
Make rs2086310(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position5146222
GeneADAMTS16
is asnp
is mentioned by
dbSNPrs2086310
ebirs2086310
HLIrs2086310
Exacrs2086310
Varsomers2086310
Maprs2086310
PheGenIrs2086310
hapmaprs2086310
1000 genomesrs2086310
hgdprs2086310
ensemblrs2086310
gopubmedrs2086310
geneviewrs2086310
scholarrs2086310
googlers2086310
pharmgkbrs2086310
gwascentralrs2086310
openSNPrs2086310
23andMers2086310
23andMe allrs2086310
SNP Nexus

SNPshotrs2086310
SNPdbers2086310
MSV3drs2086310
GWAS Ctlgrs2086310
GMAF0.3122
Max Magnitude0
? (C;C) (C;G) (G;G) 28
OMIM607510
DescA DISINTEGRIN-LIKE AND METALLOPROTEINASE WITH THROMBOSPONDIN TYPE
Variant
Relatedalso
OMIM610262
Desc
Variant
Relatedalso
[PMID 19423552OA-icon.png] Positional identification of variants of Adamts16 linked to inherited hypertension.


GET Evidence
ADAMTS16-P90A
aa_change Pro90Ala
aa_change_short P90A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.760993
summary