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rs878853082

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853082(C;G)
Make rs878853082(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position158684648
GeneETFDH
is asnp
is mentioned by
dbSNPrs878853082
ebirs878853082
HLIrs878853082
Exacrs878853082
Varsomers878853082
Maprs878853082
PheGenIrs878853082
hapmaprs878853082
1000 genomesrs878853082
hgdprs878853082
ensemblrs878853082
gopubmedrs878853082
geneviewrs878853082
scholarrs878853082
googlers878853082
pharmgkbrs878853082
gwascentralrs878853082
openSNPrs878853082
23andMers878853082
23andMe allrs878853082
SNP Nexus

SNPshotrs878853082
SNPdbers878853082
MSV3drs878853082
GWAS Ctlgrs878853082
Max Magnitude0
ClinVar
Risk rs878853082(G;G)
Alt rs878853082(G;G)
Reference rs878853082(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159605800C>G
CLNSRC
CLNACC RCV000224819.1,