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rs1057519118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519118(A;A)
Make rs1057519118(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position51236954
GeneCYP19A1
is asnp
is mentioned by
dbSNPrs1057519118
dbSNP (classic)rs1057519118
ClinGenrs1057519118
ebirs1057519118
HLIrs1057519118
Exacrs1057519118
Gnomadrs1057519118
Varsomers1057519118
LitVarrs1057519118
Maprs1057519118
PheGenIrs1057519118
Biobankrs1057519118
1000 genomesrs1057519118
hgdprs1057519118
ensemblrs1057519118
geneviewrs1057519118
scholarrs1057519118
googlers1057519118
pharmgkbrs1057519118
gwascentralrs1057519118
openSNPrs1057519118
23andMers1057519118
SNPshotrs1057519118
SNPdbers1057519118
MSV3drs1057519118
GWAS Ctlgrs1057519118
Max Magnitude0
ClinVar
Risk rs1057519118(A;A)
Alt rs1057519118(A;A)
Reference Rs1057519118(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CYP19A1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.51529151C>T
CLNSRC
CLNACC RCV000415789.1,