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rs28942091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs28942091(C;T)
Make rs28942091(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position9943452
GeneCRELD1
is asnp
is mentioned by
dbSNPrs28942091
ebirs28942091
HLIrs28942091
Exacrs28942091
Varsomers28942091
Maprs28942091
PheGenIrs28942091
hapmaprs28942091
1000 genomesrs28942091
hgdprs28942091
ensemblrs28942091
gopubmedrs28942091
geneviewrs28942091
scholarrs28942091
googlers28942091
pharmgkbrs28942091
gwascentralrs28942091
openSNPrs28942091
23andMers28942091
23andMe allrs28942091
SNP Nexus

SNPshotrs28942091
SNPdbers28942091
MSV3drs28942091
GWAS Ctlgrs28942091
GMAF0.0004591
Max Magnitude0
OMIM607170
DescATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2
Variant0001
Relatedalso
Neighborrs28942092
Distance53


ClinVar
Risk rs28942091(T;T)
Alt rs28942091(T;T)
Reference rs28942091(C;C)
Significance Other
Disease Atrioventricular septal defect 2
Variation info
Gene CRELD1
CLNDBN Atrioventricular septal defect 2
Reversed 0
HGVS NC_000003.11:g.9985136C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003596.3,