Have questions? Visit https://www.reddit.com/r/SNPedia

rs3734693

From SNPedia

Orientationplus
Stabilizedplus
Make rs3734693(C;C)
Make rs3734693(C;T)
Make rs3734693(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position43997428
is asnp
is mentioned by
dbSNPrs3734693
ebirs3734693
HLIrs3734693
Exacrs3734693
Varsomers3734693
Maprs3734693
PheGenIrs3734693
hapmaprs3734693
1000 genomesrs3734693
hgdprs3734693
ensemblrs3734693
gopubmedrs3734693
geneviewrs3734693
scholarrs3734693
googlers3734693
pharmgkbrs3734693
gwascentralrs3734693
openSNPrs3734693
23andMers3734693
23andMe allrs3734693
SNP Nexus

SNPshotrs3734693
SNPdbers3734693
MSV3drs3734693
GWAS Ctlgrs3734693
GMAF0.3981
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM612650
DescCILIARY DYSKINESIA, PRIMARY, 12; CILD12
Variant
Relatedalso
[PMID 19200523OA-icon.png] Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.