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rs376785840

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs376785840(C;C)
Make rs376785840(C;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position17181904
GeneCECR1
is asnp
is mentioned by
dbSNPrs376785840
ebirs376785840
HLIrs376785840
Exacrs376785840
Varsomers376785840
Maprs376785840
PheGenIrs376785840
hapmaprs376785840
1000 genomesrs376785840
hgdprs376785840
ensemblrs376785840
gopubmedrs376785840
geneviewrs376785840
scholarrs376785840
googlers376785840
pharmgkbrs376785840
gwascentralrs376785840
openSNPrs376785840
23andMers376785840
23andMe allrs376785840
SNP Nexus

SNPshotrs376785840
SNPdbers376785840
MSV3drs376785840
GWAS Ctlgrs376785840
Max Magnitude0
ClinVar
Risk rs376785840(C;C)
Alt rs376785840(C;C)
Reference rs376785840(T;T)
Significance Pathogenic
Disease Polyarteritis nodosa
Variation info
Gene CECR1
CLNDBN Polyarteritis nodosa
Reversed 0
HGVS NC_000022.10:g.17662794T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000106380.3,