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rs137853126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853126(G;T)
Make rs137853126(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position134606993
GeneSAR1B
is asnp
is mentioned by
dbSNPrs137853126
ebirs137853126
HLIrs137853126
Exacrs137853126
Varsomers137853126
Maprs137853126
PheGenIrs137853126
hapmaprs137853126
1000 genomesrs137853126
hgdprs137853126
ensemblrs137853126
gopubmedrs137853126
geneviewrs137853126
scholarrs137853126
googlers137853126
pharmgkbrs137853126
gwascentralrs137853126
openSNPrs137853126
23andMers137853126
23andMe allrs137853126
SNP Nexus

SNPshotrs137853126
SNPdbers137853126
MSV3drs137853126
GWAS Ctlgrs137853126
GMAF0.0004591
Max Magnitude0
OMIM607690
Desc
Variant0008
Relatedalso
ClinVar
Risk rs137853126(T;T)
Alt rs137853126(T;T)
Reference rs137853126(G;G)
Significance Pathogenic
Disease Chylomicron retention disease
Variation info
Gene SAR1B
CLNDBN Chylomicron retention disease
Reversed 1
HGVS NC_000005.9:g.133942683C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003063.2,