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rs377022708

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377022708(C;T)
Make rs377022708(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position128910051
GeneACAD9, ARHGAP11A
is asnp
is mentioned by
dbSNPrs377022708
ebirs377022708
HLIrs377022708
Exacrs377022708
Varsomers377022708
Maprs377022708
PheGenIrs377022708
hapmaprs377022708
1000 genomesrs377022708
hgdprs377022708
ensemblrs377022708
gopubmedrs377022708
geneviewrs377022708
scholarrs377022708
googlers377022708
pharmgkbrs377022708
gwascentralrs377022708
openSNPrs377022708
23andMers377022708
23andMe allrs377022708
SNP Nexus

SNPshotrs377022708
SNPdbers377022708
MSV3drs377022708
GWAS Ctlgrs377022708
Max Magnitude0
ClinVar
Risk rs377022708(T;T)
Alt rs377022708(T;T)
Reference rs377022708(C;C)
Significance Pathogenic
Disease Acyl-CoA dehydrogenase family not provided
Variation info
Gene LOC100132731 ACAD9
CLNDBN Acyl-CoA dehydrogenase family, member 9, deficiency of not provided
Reversed 0
HGVS NC_000003.11:g.128628894C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023869.3, RCV000200123.2, RCV000201606.1,