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rs796051900

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796051900(A;G)
Make rs796051900(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position75733570
GeneACADM
is asnp
is mentioned by
dbSNPrs796051900
ebirs796051900
HLIrs796051900
Exacrs796051900
Varsomers796051900
Maprs796051900
PheGenIrs796051900
hapmaprs796051900
1000 genomesrs796051900
hgdprs796051900
ensemblrs796051900
gopubmedrs796051900
geneviewrs796051900
scholarrs796051900
googlers796051900
pharmgkbrs796051900
gwascentralrs796051900
openSNPrs796051900
23andMers796051900
23andMe allrs796051900
SNP Nexus

SNPshotrs796051900
SNPdbers796051900
MSV3drs796051900
GWAS Ctlgrs796051900
Max Magnitude0
ClinVar
Risk rs796051900(G;G)
Alt rs796051900(G;G)
Reference rs796051900(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76199255A>G
CLNSRC
CLNACC RCV000185673.1,