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rs558005496

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs558005496(C;C)
Make rs558005496(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position158706254
GeneETFDH
is asnp
is mentioned by
dbSNPrs558005496
ebirs558005496
HLIrs558005496
Exacrs558005496
Varsomers558005496
Maprs558005496
PheGenIrs558005496
hapmaprs558005496
1000 genomesrs558005496
hgdprs558005496
ensemblrs558005496
gopubmedrs558005496
geneviewrs558005496
scholarrs558005496
googlers558005496
pharmgkbrs558005496
gwascentralrs558005496
openSNPrs558005496
23andMers558005496
23andMe allrs558005496
SNP Nexus

SNPshotrs558005496
SNPdbers558005496
MSV3drs558005496
GWAS Ctlgrs558005496
Max Magnitude0
ClinVar
Risk rs558005496(C;C)
Alt rs558005496(C;C)
Reference rs558005496(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159627406G>C
CLNSRC
CLNACC RCV000185899.1,