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rs587777661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777661(C;C)
Make rs587777661(C;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position31464666
GeneARMC5
is asnp
is mentioned by
dbSNPrs587777661
ebirs587777661
HLIrs587777661
Exacrs587777661
Varsomers587777661
Maprs587777661
PheGenIrs587777661
hapmaprs587777661
1000 genomesrs587777661
hgdprs587777661
ensemblrs587777661
gopubmedrs587777661
geneviewrs587777661
scholarrs587777661
googlers587777661
pharmgkbrs587777661
gwascentralrs587777661
openSNPrs587777661
23andMers587777661
23andMe allrs587777661
SNP Nexus

SNPshotrs587777661
SNPdbers587777661
MSV3drs587777661
GWAS Ctlgrs587777661
Max Magnitude0
ClinVar
Risk rs587777661(C;C)
Alt rs587777661(C;C)
Reference rs587777661(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.31475987T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133560.2,