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rs876661309

From SNPedia

Orientationplus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs876661309(-;-)
Make rs876661309(-;CCT)
Make rs876661309(CCT;CCT)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position154990458
GeneFLAD1
is asnp
is mentioned by
dbSNPrs876661309
ebirs876661309
HLIrs876661309
Exacrs876661309
Varsomers876661309
Maprs876661309
PheGenIrs876661309
hapmaprs876661309
1000 genomesrs876661309
hgdprs876661309
ensemblrs876661309
gopubmedrs876661309
geneviewrs876661309
scholarrs876661309
googlers876661309
pharmgkbrs876661309
gwascentralrs876661309
openSNPrs876661309
23andMers876661309
23andMe allrs876661309
SNP Nexus

SNPshotrs876661309
SNPdbers876661309
MSV3drs876661309
GWAS Ctlgrs876661309
Max Magnitude0
ClinVar
Risk rs876661309(;)
Alt rs876661309(;)
Reference rs876661309(CTC;CTC)
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.154962934_154962936delCCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000223940.1, RCV000234840.1,