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rs779103938

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779103938(C;T)
Make rs779103938(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position142875024
GeneCYP11B1, GML
is asnp
is mentioned by
dbSNPrs779103938
ebirs779103938
HLIrs779103938
Exacrs779103938
Varsomers779103938
Maprs779103938
PheGenIrs779103938
hapmaprs779103938
1000 genomesrs779103938
hgdprs779103938
ensemblrs779103938
gopubmedrs779103938
geneviewrs779103938
scholarrs779103938
googlers779103938
pharmgkbrs779103938
gwascentralrs779103938
openSNPrs779103938
23andMers779103938
23andMe allrs779103938
SNP Nexus

SNPshotrs779103938
SNPdbers779103938
MSV3drs779103938
GWAS Ctlgrs779103938
Max Magnitude0
ClinVar
Risk rs779103938(T;T)
Alt rs779103938(T;T)
Reference rs779103938(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CYP11B1
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.143956440C>T
CLNSRC
CLNACC RCV000224289.1,