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rs121964954

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964954(A;A)
Make rs121964954(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position158682269
GeneETFDH
is asnp
is mentioned by
dbSNPrs121964954
ebirs121964954
HLIrs121964954
Exacrs121964954
Varsomers121964954
Maprs121964954
PheGenIrs121964954
hapmaprs121964954
1000 genomesrs121964954
hgdprs121964954
ensemblrs121964954
gopubmedrs121964954
geneviewrs121964954
scholarrs121964954
googlers121964954
pharmgkbrs121964954
gwascentralrs121964954
openSNPrs121964954
23andMers121964954
23andMe allrs121964954
SNP Nexus

SNPshotrs121964954
SNPdbers121964954
MSV3drs121964954
GWAS Ctlgrs121964954
Max Magnitude0
OMIM231675
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121964954(A;A)
Alt rs121964954(A;A)
Reference rs121964954(G;G)
Significance Pathogenic
Disease Glutaric acidemia IIC not provided
Variation info
Gene ETFDH
CLNDBN Glutaric acidemia IIC not provided
Reversed 0
HGVS NC_000004.11:g.159603421G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012808.22, RCV000224728.1,