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rs776428695

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776428695(C;T)
Make rs776428695(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position158699093
GeneETFDH
is asnp
is mentioned by
dbSNPrs776428695
ebirs776428695
HLIrs776428695
Exacrs776428695
Varsomers776428695
Maprs776428695
PheGenIrs776428695
hapmaprs776428695
1000 genomesrs776428695
hgdprs776428695
ensemblrs776428695
gopubmedrs776428695
geneviewrs776428695
scholarrs776428695
googlers776428695
pharmgkbrs776428695
gwascentralrs776428695
openSNPrs776428695
23andMers776428695
23andMe allrs776428695
SNP Nexus

SNPshotrs776428695
SNPdbers776428695
MSV3drs776428695
GWAS Ctlgrs776428695
Max Magnitude0
ClinVar
Risk rs776428695(T;T)
Alt rs776428695(T;T)
Reference rs776428695(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159620245C>T
CLNSRC
CLNACC RCV000185898.2,