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rs117149381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs117149381(C;T)
Make rs117149381(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position37862001
GeneNME8
is asnp
is mentioned by
dbSNPrs117149381
ebirs117149381
HLIrs117149381
Exacrs117149381
Varsomers117149381
Maprs117149381
PheGenIrs117149381
hapmaprs117149381
1000 genomesrs117149381
hgdprs117149381
ensemblrs117149381
gopubmedrs117149381
geneviewrs117149381
scholarrs117149381
googlers117149381
pharmgkbrs117149381
gwascentralrs117149381
openSNPrs117149381
23andMers117149381
23andMe allrs117149381
SNP Nexus

SNPshotrs117149381
SNPdbers117149381
MSV3drs117149381
GWAS Ctlgrs117149381
GMAF0.008724
Max Magnitude0
ClinVar
Risk rs117149381(T;T)
Alt rs117149381(T;T)
Reference rs117149381(C;C)
Significance Other
Disease Ciliary dyskinesia
Variation info
Gene NME8
CLNDBN Ciliary dyskinesia, primary, 6
Reversed 0
HGVS NC_000007.13:g.37901603C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003413.3,