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rs279552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(G;G) 0 common in complete genomics
Make rs279552(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position9934475
GeneCRELD1
is asnp
is mentioned by
dbSNPrs279552
dbSNP (classic)rs279552
ClinGenrs279552
ebirs279552
HLIrs279552
Exacrs279552
Gnomadrs279552
Varsomers279552
LitVarrs279552
Maprs279552
PheGenIrs279552
Biobankrs279552
1000 genomesrs279552
hgdprs279552
ensemblrs279552
geneviewrs279552
scholarrs279552
googlers279552
pharmgkbrs279552
gwascentralrs279552
openSNPrs279552
23andMers279552
SNPshotrs279552
SNPdbers279552
MSV3drs279552
GWAS Ctlgrs279552
GMAF0.006428
Max Magnitude0
? (A;A) (A;G) (G;G) 28




ClinVar
Risk Rs279552(G;G)
Alt Rs279552(G;G)
Reference Rs279552(A;A)
Significance Non-pathogenic
Disease not specified Atrioventricular septal defect 2
Variation info
Gene CRELD1
CLNDBN not specified Atrioventricular septal defect 2
Reversed 0
HGVS NC_000003.11:g.9976159A\x3d
CLNSRC ClinVar GeneDx
CLNACC RCV000124609.1, RCV000462748.1,