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rs2236722

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2236722(C;C)
Make rs2236722(C;T)
ReferenceGRCh38 38.1/142
Chromosome15
Position51242798
GeneCYP19A1
is asnp
is mentioned by
dbSNPrs2236722
dbSNP (classic)rs2236722
ClinGenrs2236722
ebirs2236722
HLIrs2236722
Exacrs2236722
Gnomadrs2236722
Varsomers2236722
LitVarrs2236722
Maprs2236722
PheGenIrs2236722
Biobankrs2236722
1000 genomesrs2236722
hgdprs2236722
ensemblrs2236722
geneviewrs2236722
scholarrs2236722
googlers2236722
pharmgkbrs2236722
gwascentralrs2236722
openSNPrs2236722
23andMers2236722
SNPshotrs2236722
SNPdbers2236722
MSV3drs2236722
GWAS Ctlgrs2236722
Max Magnitude0

[PMID 24968701OA-icon.png] CYP19 gene variant confers susceptibility to endometriosis-associated infertility in Chinese women


ClinVar
Risk rs2236722(C;C)
Alt rs2236722(C;C)
Reference Rs2236722(T;T)
Significance Probable-non-pathogenic
Disease Aromatase deficiency
Variation info
Gene CYP19A1
CLNDBN Aromatase deficiency
Reversed 1
HGVS NC_000015.9:g.51534995A>G
CLNSRC
CLNACC RCV000310608.1,