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rs724159962

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs724159962(C;T)
Make rs724159962(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position13711946
GeneFAR1
is asnp
is mentioned by
dbSNPrs724159962
ebirs724159962
HLIrs724159962
Exacrs724159962
Varsomers724159962
Maprs724159962
PheGenIrs724159962
hapmaprs724159962
1000 genomesrs724159962
hgdprs724159962
ensemblrs724159962
gopubmedrs724159962
geneviewrs724159962
scholarrs724159962
googlers724159962
pharmgkbrs724159962
gwascentralrs724159962
openSNPrs724159962
23andMers724159962
23andMe allrs724159962
SNP Nexus

SNPshotrs724159962
SNPdbers724159962
MSV3drs724159962
GWAS Ctlgrs724159962
Max Magnitude0
ClinVar
Risk rs724159962(T;T)
Alt rs724159962(T;T)
Reference rs724159962(C;C)
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.13733493C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149593.3,