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rs121918360

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918360(A;C)
Make rs121918360(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position77349456
GenePDE8B
is asnp
is mentioned by
dbSNPrs121918360
ebirs121918360
HLIrs121918360
Exacrs121918360
Varsomers121918360
Maprs121918360
PheGenIrs121918360
hapmaprs121918360
1000 genomesrs121918360
hgdprs121918360
ensemblrs121918360
gopubmedrs121918360
geneviewrs121918360
scholarrs121918360
googlers121918360
pharmgkbrs121918360
gwascentralrs121918360
openSNPrs121918360
23andMers121918360
23andMe allrs121918360
SNP Nexus

SNPshotrs121918360
SNPdbers121918360
MSV3drs121918360
GWAS Ctlgrs121918360
Max Magnitude0
OMIM603390
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918360(C;C)
Alt rs121918360(C;C)
Reference rs121918360(A;A)
Significance Pathogenic
Disease Pigmented nodular adrenocortical disease
Variation info
Gene PDE8B
CLNDBN Pigmented nodular adrenocortical disease, primary, 3
Reversed 0
HGVS NC_000005.9:g.76645281A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006762.2,