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rs121917846

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917846(A;A)
Make rs121917846(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position134621002
GeneSAR1B
is asnp
is mentioned by
dbSNPrs121917846
ebirs121917846
HLIrs121917846
Exacrs121917846
Varsomers121917846
Maprs121917846
PheGenIrs121917846
hapmaprs121917846
1000 genomesrs121917846
hgdprs121917846
ensemblrs121917846
gopubmedrs121917846
geneviewrs121917846
scholarrs121917846
googlers121917846
pharmgkbrs121917846
gwascentralrs121917846
openSNPrs121917846
23andMers121917846
23andMe allrs121917846
SNP Nexus

SNPshotrs121917846
SNPdbers121917846
MSV3drs121917846
GWAS Ctlgrs121917846
Max Magnitude0
ClinVar
Risk rs121917846(A;A)
Alt rs121917846(A;A)
Reference rs121917846(G;G)
Significance Pathogenic
Disease Chylomicron retention disease
Variation info
Gene SAR1B
CLNDBN Chylomicron retention disease
Reversed 1
HGVS NC_000005.9:g.133956692C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003056.2,