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rs587777663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777663(C;C)
Make rs587777663(C;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position31462641
GeneARMC5
is asnp
is mentioned by
dbSNPrs587777663
ebirs587777663
HLIrs587777663
Exacrs587777663
Varsomers587777663
Maprs587777663
PheGenIrs587777663
hapmaprs587777663
1000 genomesrs587777663
hgdprs587777663
ensemblrs587777663
gopubmedrs587777663
geneviewrs587777663
scholarrs587777663
googlers587777663
pharmgkbrs587777663
gwascentralrs587777663
openSNPrs587777663
23andMers587777663
23andMe allrs587777663
SNP Nexus

SNPshotrs587777663
SNPdbers587777663
MSV3drs587777663
GWAS Ctlgrs587777663
Max Magnitude0
ClinVar
Risk rs587777663(C;C)
Alt rs587777663(C;C)
Reference rs587777663(T;T)
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.31473962T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133563.3,