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rs587777242

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777242(C;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position17191773
GeneCECR1
is asnp
is mentioned by
dbSNPrs587777242
ebirs587777242
HLIrs587777242
Exacrs587777242
Varsomers587777242
Maprs587777242
PheGenIrs587777242
hapmaprs587777242
1000 genomesrs587777242
hgdprs587777242
ensemblrs587777242
gopubmedrs587777242
geneviewrs587777242
scholarrs587777242
googlers587777242
pharmgkbrs587777242
gwascentralrs587777242
openSNPrs587777242
23andMers587777242
23andMe allrs587777242
SNP Nexus

SNPshotrs587777242
SNPdbers587777242
MSV3drs587777242
GWAS Ctlgrs587777242
Max Magnitude0
ClinVar
Risk rs587777242(C;C)
Alt rs587777242(C;C)
Reference rs587777242(G;G)
Significance Pathogenic
Disease Polyarteritis nodosa
Variation info
Gene CECR1
CLNDBN Polyarteritis nodosa
Reversed 1
HGVS NC_000022.10:g.17672663C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000106388.3,