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rs387906297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTT;AGTT) 0 common in clinvar
(TTAG;TTAG) 0 common in clinvar
Make rs387906297(-;-)
Make rs387906297(-;TTAG)
ReferenceGRCh38 38.1/141
Chromosome1
Position75761278
GeneACADM
is asnp
is mentioned by
dbSNPrs387906297
ebirs387906297
HLIrs387906297
Exacrs387906297
Varsomers387906297
Maprs387906297
PheGenIrs387906297
hapmaprs387906297
1000 genomesrs387906297
hgdprs387906297
ensemblrs387906297
gopubmedrs387906297
geneviewrs387906297
scholarrs387906297
googlers387906297
pharmgkbrs387906297
gwascentralrs387906297
openSNPrs387906297
23andMers387906297
23andMe allrs387906297
SNP Nexus

SNPshotrs387906297
SNPdbers387906297
MSV3drs387906297
GWAS Ctlgrs387906297
Max Magnitude0
ClinVar
Risk rs387906297(;)
Alt rs387906297(;)
Reference rs387906297(AGTT;AGTT)
Significance Pathogenic
Disease Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Variation info
Gene ACADM
CLNDBN Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000001.10:g.76226963_76226966delTTAG
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000003775.2, RCV000077877.3,