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rs766742117

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766742117(C;T)
Make rs766742117(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7224010
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs766742117
ebirs766742117
HLIrs766742117
Exacrs766742117
Varsomers766742117
Maprs766742117
PheGenIrs766742117
hapmaprs766742117
1000 genomesrs766742117
hgdprs766742117
ensemblrs766742117
gopubmedrs766742117
geneviewrs766742117
scholarrs766742117
googlers766742117
pharmgkbrs766742117
gwascentralrs766742117
openSNPrs766742117
23andMers766742117
23andMe allrs766742117
SNP Nexus

SNPshotrs766742117
SNPdbers766742117
MSV3drs766742117
GWAS Ctlgrs766742117
Max Magnitude0
ClinVar
Risk rs766742117(T;T)
Alt rs766742117(T;T)
Reference rs766742117(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADVL MIR324
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7127329C>T
CLNSRC
CLNACC RCV000185725.1,