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rs121912626

From SNPedia

Orientationplus
Stabilizedplus
Make rs121912626(C;C)
Make rs121912626(C;G)
Make rs121912626(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position9940873
GeneCRELD1
is asnp
is mentioned by
dbSNPrs121912626
dbSNP (old)rs121912626
ClinGenrs121912626
ebirs121912626
HLIrs121912626
Exacrs121912626
Gnomadrs121912626
Varsomers121912626
Maprs121912626
PheGenIrs121912626
Biobankrs121912626
1000 genomesrs121912626
hgdprs121912626
ensemblrs121912626
gopubmedrs121912626
geneviewrs121912626
scholarrs121912626
googlers121912626
pharmgkbrs121912626
gwascentralrs121912626
openSNPrs121912626
23andMers121912626
23andMe allrs121912626
SNP Nexus

SNPshotrs121912626
SNPdbers121912626
MSV3drs121912626
GWAS Ctlgrs121912626
Max Magnitude
OMIM607170
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121912626(G;G)
Alt rs121912626(G;G)
Reference rs121912626(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.9982557C>G
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000003599.2,