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rs3823884

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3823884(G;G)
Make rs3823884(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position75915137
GeneMIR4651, POR
is asnp
is mentioned by
dbSNPrs3823884
dbSNP (classic)rs3823884
ClinGenrs3823884
ebirs3823884
HLIrs3823884
Exacrs3823884
Gnomadrs3823884
Varsomers3823884
LitVarrs3823884
Maprs3823884
PheGenIrs3823884
Biobankrs3823884
1000 genomesrs3823884
hgdprs3823884
ensemblrs3823884
geneviewrs3823884
scholarrs3823884
googlers3823884
pharmgkbrs3823884
gwascentralrs3823884
openSNPrs3823884
23andMers3823884
SNPshotrs3823884
SNPdbers3823884
MSV3drs3823884
GWAS Ctlgrs3823884
Max Magnitude0

[PMID 27660057] Associations of cytochrome P450 oxidoreductase genetic polymorphisms with smoking cessation in a Chinese population.

ClinVar
Risk rs3823884(G;G)
Alt rs3823884(G;G)
Reference Rs3823884(T;T)
Significance Non-pathogenic
Disease Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
Variation info
Gene POR MIR4651
CLNDBN Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
Reversed 1
HGVS NC_000007.13:g.75544455A>C
CLNSRC
CLNACC RCV000379412.1,