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rs724159963

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs724159963(A;G)
Make rs724159963(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position13714647
GeneFAR1
is asnp
is mentioned by
dbSNPrs724159963
ebirs724159963
HLIrs724159963
Exacrs724159963
Varsomers724159963
Maprs724159963
PheGenIrs724159963
hapmaprs724159963
1000 genomesrs724159963
hgdprs724159963
ensemblrs724159963
gopubmedrs724159963
geneviewrs724159963
scholarrs724159963
googlers724159963
pharmgkbrs724159963
gwascentralrs724159963
openSNPrs724159963
23andMers724159963
23andMe allrs724159963
SNP Nexus

SNPshotrs724159963
SNPdbers724159963
MSV3drs724159963
GWAS Ctlgrs724159963
Max Magnitude0
ClinVar
Risk rs724159963(G;G)
Alt rs724159963(G;G)
Reference rs724159963(A;A)
Significance Pathogenic
Disease Peroxisomal fatty acyl-coa reductase 1 disorder
Variation info
Gene FAR1
CLNDBN Peroxisomal fatty acyl-coa reductase 1 disorder
Reversed 0
HGVS NC_000011.9:g.13736194A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000149594.4,