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rs766140986

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766140986(C;T)
Make rs766140986(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75761228
GeneACADM
is asnp
is mentioned by
dbSNPrs766140986
ebirs766140986
HLIrs766140986
Exacrs766140986
Varsomers766140986
Maprs766140986
PheGenIrs766140986
hapmaprs766140986
1000 genomesrs766140986
hgdprs766140986
ensemblrs766140986
gopubmedrs766140986
geneviewrs766140986
scholarrs766140986
googlers766140986
pharmgkbrs766140986
gwascentralrs766140986
openSNPrs766140986
23andMers766140986
23andMe allrs766140986
SNP Nexus

SNPshotrs766140986
SNPdbers766140986
MSV3drs766140986
GWAS Ctlgrs766140986
Max Magnitude0
ClinVar
Risk rs766140986(T;T)
Alt rs766140986(T;T)
Reference rs766140986(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76226913C>T
CLNSRC
CLNACC RCV000185667.2,