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rs786205107

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205107(C;C)
Make rs786205107(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position51218539
GeneCYP19A1, PIRC66
is asnp
is mentioned by
dbSNPrs786205107
ebirs786205107
HLIrs786205107
Exacrs786205107
Varsomers786205107
Maprs786205107
PheGenIrs786205107
hapmaprs786205107
1000 genomesrs786205107
hgdprs786205107
ensemblrs786205107
gopubmedrs786205107
geneviewrs786205107
scholarrs786205107
googlers786205107
pharmgkbrs786205107
gwascentralrs786205107
openSNPrs786205107
23andMers786205107
23andMe allrs786205107
SNP Nexus

SNPshotrs786205107
SNPdbers786205107
MSV3drs786205107
GWAS Ctlgrs786205107
Max Magnitude0
ClinVar
Risk rs786205107(C;C)
Alt rs786205107(C;C)
Reference rs786205107(T;T)
Significance Pathogenic
Disease Aromatase deficiency
Variation info
Gene CYP19A1
CLNDBN Aromatase deficiency
Reversed 1
HGVS NC_000015.9:g.51510736A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019395.28,