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rs200930463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200930463(C;G)
Make rs200930463(G;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position17209538
GeneCECR1
is asnp
is mentioned by
dbSNPrs200930463
ebirs200930463
HLIrs200930463
Exacrs200930463
Varsomers200930463
Maprs200930463
PheGenIrs200930463
hapmaprs200930463
1000 genomesrs200930463
hgdprs200930463
ensemblrs200930463
gopubmedrs200930463
geneviewrs200930463
scholarrs200930463
googlers200930463
pharmgkbrs200930463
gwascentralrs200930463
openSNPrs200930463
23andMers200930463
23andMe allrs200930463
SNP Nexus

SNPshotrs200930463
SNPdbers200930463
MSV3drs200930463
GWAS Ctlgrs200930463
Max Magnitude0
ClinVar
Risk rs200930463(A,G;A,G)
Alt rs200930463(A,G;A,G)
Reference rs200930463(C;C)
Significance Pathogenic
Disease Polyarteritis nodosa
Variation info
Gene CECR1
CLNDBN Polyarteritis nodosa
Reversed 0
HGVS NC_000022.10:g.17690428C>A; NC_000022.10:g.17690428C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000106387.3, RCV000106382.3,