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rs1057518574

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518574(C;C)
Make rs1057518574(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position51227850
GeneCYP19A1
is asnp
is mentioned by
dbSNPrs1057518574
dbSNP (old)rs1057518574
ClinGenrs1057518574
ebirs1057518574
HLIrs1057518574
Exacrs1057518574
Gnomadrs1057518574
Varsomers1057518574
LitVarrs1057518574
Maprs1057518574
PheGenIrs1057518574
Biobankrs1057518574
1000 genomesrs1057518574
hgdprs1057518574
ensemblrs1057518574
gopubmedrs1057518574
geneviewrs1057518574
scholarrs1057518574
googlers1057518574
pharmgkbrs1057518574
gwascentralrs1057518574
openSNPrs1057518574
23andMers1057518574
23andMe allrs1057518574
SNPshotrs1057518574
SNPdbers1057518574
MSV3drs1057518574
GWAS Ctlgrs1057518574
Max Magnitude0
ClinVar
Risk rs1057518574(C;C)
Alt rs1057518574(C;C)
Reference Rs1057518574(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CYP19A1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.51520047A>G
CLNSRC
CLNACC RCV000414127.1,