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rs377656387

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377656387(C;T)
Make rs377656387(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position158706351
GeneETFDH
is asnp
is mentioned by
dbSNPrs377656387
ebirs377656387
HLIrs377656387
Exacrs377656387
Varsomers377656387
Maprs377656387
PheGenIrs377656387
hapmaprs377656387
1000 genomesrs377656387
hgdprs377656387
ensemblrs377656387
gopubmedrs377656387
geneviewrs377656387
scholarrs377656387
googlers377656387
pharmgkbrs377656387
gwascentralrs377656387
openSNPrs377656387
23andMers377656387
23andMe allrs377656387
SNP Nexus

SNPshotrs377656387
SNPdbers377656387
MSV3drs377656387
GWAS Ctlgrs377656387
Max Magnitude0
ClinVar
Risk rs377656387(T;T)
Alt rs377656387(T;T)
Reference rs377656387(C;C)
Significance Pathogenic
Disease Glutaric acidemia iic
Variation info
Gene ETFDH
CLNDBN Glutaric acidemia iic, late-onset
Reversed 0
HGVS NC_000004.11:g.159627503C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024306.16,