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rs77563738

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77563738(C;T)
Make rs77563738(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position17207107
GeneCECR1
is asnp
is mentioned by
dbSNPrs77563738
ebirs77563738
HLIrs77563738
Exacrs77563738
Varsomers77563738
Maprs77563738
PheGenIrs77563738
hapmaprs77563738
1000 genomesrs77563738
hgdprs77563738
ensemblrs77563738
gopubmedrs77563738
geneviewrs77563738
scholarrs77563738
googlers77563738
pharmgkbrs77563738
gwascentralrs77563738
openSNPrs77563738
23andMers77563738
23andMe allrs77563738
SNP Nexus

SNPshotrs77563738
SNPdbers77563738
MSV3drs77563738
GWAS Ctlgrs77563738
Max Magnitude0
ClinVar
Risk rs77563738(G,T;G,T)
Alt rs77563738(G,T;G,T)
Reference rs77563738(C;C)
Significance Pathogenic
Disease Polyarteritis nodosa
Variation info
Gene CECR1
CLNDBN Polyarteritis nodosa
Reversed 0
HGVS NC_000022.10:g.17687997C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000106384.3,