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rs371260517

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371260517(A;A)
Make rs371260517(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position158695545
GeneETFDH
is asnp
is mentioned by
dbSNPrs371260517
ebirs371260517
HLIrs371260517
Exacrs371260517
Varsomers371260517
Maprs371260517
PheGenIrs371260517
hapmaprs371260517
1000 genomesrs371260517
hgdprs371260517
ensemblrs371260517
gopubmedrs371260517
geneviewrs371260517
scholarrs371260517
googlers371260517
pharmgkbrs371260517
gwascentralrs371260517
openSNPrs371260517
23andMers371260517
23andMe allrs371260517
SNP Nexus

SNPshotrs371260517
SNPdbers371260517
MSV3drs371260517
GWAS Ctlgrs371260517
Max Magnitude0
ClinVar
Risk rs371260517(A;A)
Alt rs371260517(A;A)
Reference rs371260517(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159616697G>A
CLNSRC
CLNACC RCV000185893.1,