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rs587777199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777199(A;A)
Make rs587777199(A;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position27940577
GeneARMC4
is asnp
is mentioned by
dbSNPrs587777199
ebirs587777199
HLIrs587777199
Exacrs587777199
Varsomers587777199
Maprs587777199
PheGenIrs587777199
hapmaprs587777199
1000 genomesrs587777199
hgdprs587777199
ensemblrs587777199
gopubmedrs587777199
geneviewrs587777199
scholarrs587777199
googlers587777199
pharmgkbrs587777199
gwascentralrs587777199
openSNPrs587777199
23andMers587777199
23andMe allrs587777199
SNP Nexus

SNPshotrs587777199
SNPdbers587777199
MSV3drs587777199
GWAS Ctlgrs587777199
Max Magnitude0
ClinVar
Risk rs587777199(A;A)
Alt rs587777199(A;A)
Reference rs587777199(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia 23
Variation info
Gene ARMC4
CLNDBN Primary ciliary dyskinesia 23
Reversed 0
HGVS NC_000010.10:g.28229506C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087327.3,