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rs61752786

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61752786(A;A)
Make rs61752786(A;C)
ReferenceGRCh38 38.1/142
Chromosome8
Position142875713
GeneCYP11B1
is asnp
is mentioned by
dbSNPrs61752786
ebirs61752786
HLIrs61752786
Exacrs61752786
Varsomers61752786
Maprs61752786
PheGenIrs61752786
hapmaprs61752786
1000 genomesrs61752786
hgdprs61752786
ensemblrs61752786
gopubmedrs61752786
geneviewrs61752786
scholarrs61752786
googlers61752786
pharmgkbrs61752786
gwascentralrs61752786
openSNPrs61752786
23andMers61752786
23andMe allrs61752786
SNP Nexus

SNPshotrs61752786
SNPdbers61752786
MSV3drs61752786
GWAS Ctlgrs61752786
GMAF0.007346
Max Magnitude0
ClinVar
Risk rs61752786(A,T;A,T)
Alt rs61752786(A,T;A,T)
Reference rs61752786(C;C)
Significance Probable-Pathogenic
Disease Congenital adrenal hyperplasia
Variation info
Gene CYP11B1
CLNDBN Congenital adrenal hyperplasia
Reversed 1
HGVS NC_000008.10:g.143957129G>A; NC_000008.10:g.143957129G>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029638.1, RCV000029637.1,