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rs767795266

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs767795266(-;-)
Make rs767795266(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position158708446
GeneETFDH
is asnp
is mentioned by
dbSNPrs767795266
ebirs767795266
HLIrs767795266
Exacrs767795266
Varsomers767795266
Maprs767795266
PheGenIrs767795266
hapmaprs767795266
1000 genomesrs767795266
hgdprs767795266
ensemblrs767795266
gopubmedrs767795266
geneviewrs767795266
scholarrs767795266
googlers767795266
pharmgkbrs767795266
gwascentralrs767795266
openSNPrs767795266
23andMers767795266
23andMe allrs767795266
SNP Nexus

SNPshotrs767795266
SNPdbers767795266
MSV3drs767795266
GWAS Ctlgrs767795266
Max Magnitude0
ClinVar
Risk rs767795266(;)
Alt rs767795266(;)
Reference rs767795266(AT;AT)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159629598_159629599delAT
CLNSRC
CLNACC RCV000224798.1,