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rs28939089

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28939089(C;C)
Make rs28939089(C;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position77032304
GenePSTPIP1
is asnp
is mentioned by
dbSNPrs28939089
ebirs28939089
HLIrs28939089
Exacrs28939089
Varsomers28939089
Maprs28939089
PheGenIrs28939089
hapmaprs28939089
1000 genomesrs28939089
hgdprs28939089
ensemblrs28939089
gopubmedrs28939089
geneviewrs28939089
scholarrs28939089
googlers28939089
pharmgkbrs28939089
gwascentralrs28939089
openSNPrs28939089
23andMers28939089
23andMe allrs28939089
SNP Nexus

SNPshotrs28939089
SNPdbers28939089
MSV3drs28939089
GWAS Ctlgrs28939089
Max Magnitude0
OMIM606347
DescPYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE
Variant0001
Relatedalso
ClinVar
Risk rs28939089(A,C;A,C)
Alt rs28939089(A,C;A,C)
Reference rs28939089(G;G)
Significance Pathogenic
Disease Pyogenic arthritis not provided
Variation info
Gene PSTPIP1
CLNDBN Pyogenic arthritis, pyoderma gangrenosum and acne not provided
Reversed 0
HGVS NC_000015.9:g.77324645G>A; NC_000015.9:g.77324645G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000084063.1, RCV000215780.1, RCV000004684.2,