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rs771874163

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771874163(C;T)
Make rs771874163(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7223151
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs771874163
ebirs771874163
HLIrs771874163
Exacrs771874163
Varsomers771874163
Maprs771874163
PheGenIrs771874163
hapmaprs771874163
1000 genomesrs771874163
hgdprs771874163
ensemblrs771874163
gopubmedrs771874163
geneviewrs771874163
scholarrs771874163
googlers771874163
pharmgkbrs771874163
gwascentralrs771874163
openSNPrs771874163
23andMers771874163
23andMe allrs771874163
SNP Nexus

SNPshotrs771874163
SNPdbers771874163
MSV3drs771874163
GWAS Ctlgrs771874163
Max Magnitude0
ClinVar
Risk rs771874163(G,T;G,T)
Alt rs771874163(G,T;G,T)
Reference rs771874163(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADVL MIR324
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7126470C>T
CLNSRC
CLNACC RCV000185719.2,