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rs587777049

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777049(G;T)
Make rs587777049(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position27862558
GeneARMC4
is asnp
is mentioned by
dbSNPrs587777049
ebirs587777049
HLIrs587777049
Exacrs587777049
Varsomers587777049
Maprs587777049
PheGenIrs587777049
hapmaprs587777049
1000 genomesrs587777049
hgdprs587777049
ensemblrs587777049
gopubmedrs587777049
geneviewrs587777049
scholarrs587777049
googlers587777049
pharmgkbrs587777049
gwascentralrs587777049
openSNPrs587777049
23andMers587777049
23andMe allrs587777049
SNP Nexus

SNPshotrs587777049
SNPdbers587777049
MSV3drs587777049
GWAS Ctlgrs587777049
Max Magnitude0
ClinVar
Risk rs587777049(G,T;G,T)
Alt rs587777049(G,T;G,T)
Reference rs587777049(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia 23
Variation info
Gene ARMC4
CLNDBN Primary ciliary dyskinesia 23
Reversed 1
HGVS NC_000010.10:g.28151487G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000056286.3,