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rs765742496

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs765742496(C;C)
Make rs765742496(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position158708525
GeneETFDH
is asnp
is mentioned by
dbSNPrs765742496
ebirs765742496
HLIrs765742496
Exacrs765742496
Varsomers765742496
Maprs765742496
PheGenIrs765742496
hapmaprs765742496
1000 genomesrs765742496
hgdprs765742496
ensemblrs765742496
gopubmedrs765742496
geneviewrs765742496
scholarrs765742496
googlers765742496
pharmgkbrs765742496
gwascentralrs765742496
openSNPrs765742496
23andMers765742496
23andMe allrs765742496
SNP Nexus

SNPshotrs765742496
SNPdbers765742496
MSV3drs765742496
GWAS Ctlgrs765742496
Max Magnitude0
ClinVar
Risk rs765742496(C;C)
Alt rs765742496(C;C)
Reference rs765742496(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159629677T>C
CLNSRC
CLNACC RCV000185902.1,