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rs137853125

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853125(G;T)
Make rs137853125(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position134608488
GeneSAR1B
is asnp
is mentioned by
dbSNPrs137853125
ebirs137853125
HLIrs137853125
Exacrs137853125
Varsomers137853125
Maprs137853125
PheGenIrs137853125
hapmaprs137853125
1000 genomesrs137853125
hgdprs137853125
ensemblrs137853125
gopubmedrs137853125
geneviewrs137853125
scholarrs137853125
googlers137853125
pharmgkbrs137853125
gwascentralrs137853125
openSNPrs137853125
23andMers137853125
23andMe allrs137853125
SNP Nexus

SNPshotrs137853125
SNPdbers137853125
MSV3drs137853125
GWAS Ctlgrs137853125
Max Magnitude0
OMIM607690
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137853125(T;T)
Alt rs137853125(T;T)
Reference rs137853125(G;G)
Significance Pathogenic
Disease Chylomicron retention disease
Variation info
Gene SAR1B
CLNDBN Chylomicron retention disease
Reversed 1
HGVS NC_000005.9:g.133944178C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003062.2,