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rs587777662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777662(C;T)
Make rs587777662(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position31464800
GeneARMC5
is asnp
is mentioned by
dbSNPrs587777662
ebirs587777662
HLIrs587777662
Exacrs587777662
Varsomers587777662
Maprs587777662
PheGenIrs587777662
hapmaprs587777662
1000 genomesrs587777662
hgdprs587777662
ensemblrs587777662
gopubmedrs587777662
geneviewrs587777662
scholarrs587777662
googlers587777662
pharmgkbrs587777662
gwascentralrs587777662
openSNPrs587777662
23andMers587777662
23andMe allrs587777662
SNP Nexus

SNPshotrs587777662
SNPdbers587777662
MSV3drs587777662
GWAS Ctlgrs587777662
Max Magnitude0
ClinVar
Risk rs587777662(T;T)
Alt rs587777662(T;T)
Reference rs587777662(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.31476121C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000133562.2,