Have questions? Visit https://www.reddit.com/r/SNPedia

rs369721476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369721476(C;T)
Make rs369721476(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position31462346
GeneARMC5
is asnp
is mentioned by
dbSNPrs369721476
ebirs369721476
HLIrs369721476
Exacrs369721476
Varsomers369721476
Maprs369721476
PheGenIrs369721476
hapmaprs369721476
1000 genomesrs369721476
hgdprs369721476
ensemblrs369721476
gopubmedrs369721476
geneviewrs369721476
scholarrs369721476
googlers369721476
pharmgkbrs369721476
gwascentralrs369721476
openSNPrs369721476
23andMers369721476
23andMe allrs369721476
SNP Nexus

SNPshotrs369721476
SNPdbers369721476
MSV3drs369721476
GWAS Ctlgrs369721476
Max Magnitude0
ClinVar
Risk rs369721476(T;T)
Alt rs369721476(T;T)
Reference rs369721476(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.31473667C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000133557.2,