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rs587777048

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777048(-;-)
Make rs587777048(-;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position27862521
GeneARMC4
is asnp
is mentioned by
dbSNPrs587777048
ebirs587777048
HLIrs587777048
Exacrs587777048
Varsomers587777048
Maprs587777048
PheGenIrs587777048
hapmaprs587777048
1000 genomesrs587777048
hgdprs587777048
ensemblrs587777048
gopubmedrs587777048
geneviewrs587777048
scholarrs587777048
googlers587777048
pharmgkbrs587777048
gwascentralrs587777048
openSNPrs587777048
23andMers587777048
23andMe allrs587777048
SNP Nexus

SNPshotrs587777048
SNPdbers587777048
MSV3drs587777048
GWAS Ctlgrs587777048
Max Magnitude0
ClinVar
Risk rs587777048(GA,A;GA,A)
Alt rs587777048(GA,A;GA,A)
Reference rs587777048(CA;CA)
Significance Pathogenic
Disease Primary ciliary dyskinesia 23
Variation info
Gene ARMC4
CLNDBN Primary ciliary dyskinesia 23
Reversed 1
HGVS NC_000010.10:g.28151450delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000056285.2,