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rs587777660

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777660(C;T)
Make rs587777660(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position31459780
GeneARMC5
is asnp
is mentioned by
dbSNPrs587777660
ebirs587777660
HLIrs587777660
Exacrs587777660
Varsomers587777660
Maprs587777660
PheGenIrs587777660
hapmaprs587777660
1000 genomesrs587777660
hgdprs587777660
ensemblrs587777660
gopubmedrs587777660
geneviewrs587777660
scholarrs587777660
googlers587777660
pharmgkbrs587777660
gwascentralrs587777660
openSNPrs587777660
23andMers587777660
23andMe allrs587777660
SNP Nexus

SNPshotrs587777660
SNPdbers587777660
MSV3drs587777660
GWAS Ctlgrs587777660
Max Magnitude0
ClinVar
Risk rs587777660(T;T)
Alt rs587777660(T;T)
Reference rs587777660(C;C)
Significance Pathogenic
Disease Acth-independent macronodular adrenal hyperplasia 2
Variation info
Gene ARMC5
CLNDBN Acth-independent macronodular adrenal hyperplasia 2
Reversed 0
HGVS NC_000016.9:g.31471101C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000133559.2,