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rs786205108

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205108(-;-)
Make rs786205108(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position51212359
GeneCYP19A1, PIRC66
is asnp
is mentioned by
dbSNPrs786205108
ebirs786205108
HLIrs786205108
Exacrs786205108
Varsomers786205108
Maprs786205108
PheGenIrs786205108
hapmaprs786205108
1000 genomesrs786205108
hgdprs786205108
ensemblrs786205108
gopubmedrs786205108
geneviewrs786205108
scholarrs786205108
googlers786205108
pharmgkbrs786205108
gwascentralrs786205108
openSNPrs786205108
23andMers786205108
23andMe allrs786205108
SNP Nexus

SNPshotrs786205108
SNPdbers786205108
MSV3drs786205108
GWAS Ctlgrs786205108
Max Magnitude0
ClinVar
Risk rs786205108(;)
Alt rs786205108(;)
Reference rs786205108(C;C)
Significance Pathogenic
Disease Aromatase deficiency
Variation info
Gene CYP19A1
CLNDBN Aromatase deficiency
Reversed 1
HGVS NC_000015.9:g.51504556delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000019397.24,