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rs121912627

From SNPedia

Orientationplus
Stabilizedplus
Make rs121912627(A;A)
Make rs121912627(A;G)
Make rs121912627(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position9944556
GeneCRELD1
is asnp
is mentioned by
dbSNPrs121912627
dbSNP (old)rs121912627
ClinGenrs121912627
ebirs121912627
HLIrs121912627
Exacrs121912627
Gnomadrs121912627
Varsomers121912627
Maprs121912627
PheGenIrs121912627
Biobankrs121912627
1000 genomesrs121912627
hgdprs121912627
ensemblrs121912627
gopubmedrs121912627
geneviewrs121912627
scholarrs121912627
googlers121912627
pharmgkbrs121912627
gwascentralrs121912627
openSNPrs121912627
23andMers121912627
23andMe allrs121912627
SNP Nexus

SNPshotrs121912627
SNPdbers121912627
MSV3drs121912627
GWAS Ctlgrs121912627
Max Magnitude
OMIM607170
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121912627(A;A)
Alt rs121912627(A;A)
Reference rs121912627(G;G)
Significance Other
Disease Atrioventricular septal defect 2
Variation info
Gene CRELD1
CLNDBN Atrioventricular septal defect 2
Reversed 0
HGVS NC_000003.11:g.9986240G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003600.2,