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rs587777659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777659(C;T)
Make rs587777659(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position31466773
GeneARMC5
is asnp
is mentioned by
dbSNPrs587777659
ebirs587777659
HLIrs587777659
Exacrs587777659
Varsomers587777659
Maprs587777659
PheGenIrs587777659
hapmaprs587777659
1000 genomesrs587777659
hgdprs587777659
ensemblrs587777659
gopubmedrs587777659
geneviewrs587777659
scholarrs587777659
googlers587777659
pharmgkbrs587777659
gwascentralrs587777659
openSNPrs587777659
23andMers587777659
23andMe allrs587777659
SNP Nexus

SNPshotrs587777659
SNPdbers587777659
MSV3drs587777659
GWAS Ctlgrs587777659
Max Magnitude0
ClinVar
Risk rs587777659(T;T)
Alt rs587777659(T;T)
Reference rs587777659(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.31478094C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000133558.2,