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rs876661311

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661311(-;-)
Make rs876661311(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position154988568
GeneFLAD1
is asnp
is mentioned by
dbSNPrs876661311
ebirs876661311
HLIrs876661311
Exacrs876661311
Varsomers876661311
Maprs876661311
PheGenIrs876661311
hapmaprs876661311
1000 genomesrs876661311
hgdprs876661311
ensemblrs876661311
gopubmedrs876661311
geneviewrs876661311
scholarrs876661311
googlers876661311
pharmgkbrs876661311
gwascentralrs876661311
openSNPrs876661311
23andMers876661311
23andMe allrs876661311
SNP Nexus

SNPshotrs876661311
SNPdbers876661311
MSV3drs876661311
GWAS Ctlgrs876661311
Max Magnitude0
ClinVar
Risk rs876661311(;)
Alt rs876661311(;)
Reference rs876661311(T;T)
Significance Pathogenic
Disease Glutaric aciduria Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency
Variation info
Gene FLAD1
CLNDBN Glutaric aciduria, type 2 Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency
Reversed 0
HGVS NC_000001.10:g.154961044delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000223939.1, RCV000234842.1,