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rs145742175

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145742175(C;T)
Make rs145742175(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position27944296
GeneARMC4
is asnp
is mentioned by
dbSNPrs145742175
ebirs145742175
HLIrs145742175
Exacrs145742175
Varsomers145742175
Maprs145742175
PheGenIrs145742175
hapmaprs145742175
1000 genomesrs145742175
hgdprs145742175
ensemblrs145742175
gopubmedrs145742175
geneviewrs145742175
scholarrs145742175
googlers145742175
pharmgkbrs145742175
gwascentralrs145742175
openSNPrs145742175
23andMers145742175
23andMe allrs145742175
SNP Nexus

SNPshotrs145742175
SNPdbers145742175
MSV3drs145742175
GWAS Ctlgrs145742175
Max Magnitude0
ClinVar
Risk rs145742175(A,T;A,T)
Alt rs145742175(A,T;A,T)
Reference rs145742175(C;C)
Significance Pathogenic
Disease Kartagener syndrome Primary ciliary dyskinesia 23
Variation info
Gene ARMC4
CLNDBN Kartagener syndrome Primary ciliary dyskinesia 23
Reversed 0
HGVS NC_000010.10:g.28233225C>A
CLNSRC
CLNACC RCV000190921.1, RCV000234898.1,