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rs549454407

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs549454407(A;A)
Make rs549454407(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position158698987
GeneETFDH
is asnp
is mentioned by
dbSNPrs549454407
ebirs549454407
HLIrs549454407
Exacrs549454407
Varsomers549454407
Maprs549454407
PheGenIrs549454407
hapmaprs549454407
1000 genomesrs549454407
hgdprs549454407
ensemblrs549454407
gopubmedrs549454407
geneviewrs549454407
scholarrs549454407
googlers549454407
pharmgkbrs549454407
gwascentralrs549454407
openSNPrs549454407
23andMers549454407
23andMe allrs549454407
SNP Nexus

SNPshotrs549454407
SNPdbers549454407
MSV3drs549454407
GWAS Ctlgrs549454407
Max Magnitude0
ClinVar
Risk rs549454407(A;A)
Alt rs549454407(A;A)
Reference rs549454407(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159620139G>T
CLNSRC
CLNACC RCV000185896.1,