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rs148936893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148936893(A;A)
Make rs148936893(A;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position17203564
GeneCECR1
is asnp
is mentioned by
dbSNPrs148936893
ebirs148936893
HLIrs148936893
Exacrs148936893
Varsomers148936893
Maprs148936893
PheGenIrs148936893
hapmaprs148936893
1000 genomesrs148936893
hgdprs148936893
ensemblrs148936893
gopubmedrs148936893
geneviewrs148936893
scholarrs148936893
googlers148936893
pharmgkbrs148936893
gwascentralrs148936893
openSNPrs148936893
23andMers148936893
23andMe allrs148936893
SNP Nexus

SNPshotrs148936893
SNPdbers148936893
MSV3drs148936893
GWAS Ctlgrs148936893
Max Magnitude0
ClinVar
Risk rs148936893(A;A)
Alt rs148936893(A;A)
Reference rs148936893(G;G)
Significance Pathogenic
Disease Polyarteritis nodosa
Variation info
Gene CECR1
CLNDBN Polyarteritis nodosa
Reversed 0
HGVS NC_000022.10:g.17684454G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000106386.3,