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rs878853006

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853006(A;T)
Make rs878853006(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position158680589
GeneETFDH
is asnp
is mentioned by
dbSNPrs878853006
ebirs878853006
HLIrs878853006
Exacrs878853006
Varsomers878853006
Maprs878853006
PheGenIrs878853006
hapmaprs878853006
1000 genomesrs878853006
hgdprs878853006
ensemblrs878853006
gopubmedrs878853006
geneviewrs878853006
scholarrs878853006
googlers878853006
pharmgkbrs878853006
gwascentralrs878853006
openSNPrs878853006
23andMers878853006
23andMe allrs878853006
SNP Nexus

SNPshotrs878853006
SNPdbers878853006
MSV3drs878853006
GWAS Ctlgrs878853006
Max Magnitude0
ClinVar
Risk rs878853006(T;T)
Alt rs878853006(T;T)
Reference rs878853006(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159601741A>T
CLNSRC
CLNACC RCV000224742.1,