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rs879253744

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253744(A;A)
Make rs879253744(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position27935009
GeneARMC4
is asnp
is mentioned by
dbSNPrs879253744
ClinGenrs879253744
ebirs879253744
HLIrs879253744
Exacrs879253744
Varsomers879253744
Maprs879253744
PheGenIrs879253744
hapmaprs879253744
1000 genomesrs879253744
hgdprs879253744
ensemblrs879253744
gopubmedrs879253744
geneviewrs879253744
scholarrs879253744
googlers879253744
pharmgkbrs879253744
gwascentralrs879253744
openSNPrs879253744
23andMers879253744
23andMe allrs879253744
SNP Nexus

SNPshotrs879253744
SNPdbers879253744
MSV3drs879253744
GWAS Ctlgrs879253744
Max Magnitude0
ClinVar
Risk rs879253744(A;A)
Alt rs879253744(A;A)
Reference Rs879253744(G;G)
Significance Pathogenic
Disease Primary ciliary dyskinesia 23
Variation info
Gene ARMC4
CLNDBN Primary ciliary dyskinesia 23
Reversed 1
HGVS NC_000010.10:g.28223938C>T
CLNSRC
CLNACC RCV000234915.1,