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rs786204642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTGA;CTGA) 0 common/normal
(TGAC;TGAC) 0 common in clinvar
Make rs786204642(-;-)
Make rs786204642(-;CTGA)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position75734852
GeneACADM
is asnp
is mentioned by
dbSNPrs786204642
ebirs786204642
HLIrs786204642
Exacrs786204642
Varsomers786204642
Maprs786204642
PheGenIrs786204642
hapmaprs786204642
1000 genomesrs786204642
hgdprs786204642
ensemblrs786204642
gopubmedrs786204642
geneviewrs786204642
scholarrs786204642
googlers786204642
pharmgkbrs786204642
gwascentralrs786204642
openSNPrs786204642
23andMers786204642
23andMe allrs786204642
SNP Nexus

SNPshotrs786204642
SNPdbers786204642
MSV3drs786204642
GWAS Ctlgrs786204642
Max Magnitude0
ClinVar
Risk rs786204642(;)
Alt rs786204642(;)
Reference rs786204642(TGAC;TGAC)
Significance Other
Disease Medium-chain acyl-coenzyme A dehydrogenase deficiency
Variation info
Gene ACADM
CLNDBN Medium-chain acyl-coenzyme A dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.76200537_76200540delCTGA
CLNSRC Counsyl
CLNACC RCV000169427.2,