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rs786205110

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205110(A;A)
Make rs786205110(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position51218658
GeneCYP19A1, PIRC66
is asnp
is mentioned by
dbSNPrs786205110
ebirs786205110
HLIrs786205110
Exacrs786205110
Varsomers786205110
Maprs786205110
PheGenIrs786205110
hapmaprs786205110
1000 genomesrs786205110
hgdprs786205110
ensemblrs786205110
gopubmedrs786205110
geneviewrs786205110
scholarrs786205110
googlers786205110
pharmgkbrs786205110
gwascentralrs786205110
openSNPrs786205110
23andMers786205110
23andMe allrs786205110
SNP Nexus

SNPshotrs786205110
SNPdbers786205110
MSV3drs786205110
GWAS Ctlgrs786205110
Max Magnitude0
ClinVar
Risk rs786205110(A;A)
Alt rs786205110(A;A)
Reference rs786205110(C;C)
Significance Pathogenic
Disease Aromatase deficiency
Variation info
Gene CYP19A1
CLNDBN Aromatase deficiency
Reversed 1
HGVS NC_000015.9:g.51510855G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019401.29,