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rs878852988

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878852988(A;A)
Make rs878852988(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position142912578
GeneCYP11B2, GML
is asnp
is mentioned by
dbSNPrs878852988
ebirs878852988
HLIrs878852988
Exacrs878852988
Varsomers878852988
Maprs878852988
PheGenIrs878852988
hapmaprs878852988
1000 genomesrs878852988
hgdprs878852988
ensemblrs878852988
gopubmedrs878852988
geneviewrs878852988
scholarrs878852988
googlers878852988
pharmgkbrs878852988
gwascentralrs878852988
openSNPrs878852988
23andMers878852988
23andMe allrs878852988
SNP Nexus

SNPshotrs878852988
SNPdbers878852988
MSV3drs878852988
GWAS Ctlgrs878852988
Max Magnitude0
ClinVar
Risk rs878852988(A;A)
Alt rs878852988(A;A)
Reference rs878852988(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CYP11B2
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.143993994G>T
CLNSRC
CLNACC RCV000224086.1,