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rs758218892

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758218892(C;C)
Make rs758218892(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position158695551
GeneETFDH
is asnp
is mentioned by
dbSNPrs758218892
ebirs758218892
HLIrs758218892
Exacrs758218892
Varsomers758218892
Maprs758218892
PheGenIrs758218892
hapmaprs758218892
1000 genomesrs758218892
hgdprs758218892
ensemblrs758218892
gopubmedrs758218892
geneviewrs758218892
scholarrs758218892
googlers758218892
pharmgkbrs758218892
gwascentralrs758218892
openSNPrs758218892
23andMers758218892
23andMe allrs758218892
SNP Nexus

SNPshotrs758218892
SNPdbers758218892
MSV3drs758218892
GWAS Ctlgrs758218892
Max Magnitude0
ClinVar
Risk rs758218892(C;C)
Alt rs758218892(C;C)
Reference rs758218892(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159616703G>C
CLNSRC
CLNACC RCV000185894.1,