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rs762664261

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs762664261(A;C)
Make rs762664261(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position80099525
GeneCCDC40
is asnp
is mentioned by
dbSNPrs762664261
ebirs762664261
HLIrs762664261
Exacrs762664261
Varsomers762664261
Maprs762664261
PheGenIrs762664261
hapmaprs762664261
1000 genomesrs762664261
hgdprs762664261
ensemblrs762664261
gopubmedrs762664261
geneviewrs762664261
scholarrs762664261
googlers762664261
pharmgkbrs762664261
gwascentralrs762664261
openSNPrs762664261
23andMers762664261
23andMe allrs762664261
SNP Nexus

SNPshotrs762664261
SNPdbers762664261
MSV3drs762664261
GWAS Ctlgrs762664261
Max Magnitude0
ClinVar
Risk rs762664261(C;C)
Alt rs762664261(C;C)
Reference rs762664261(A;A)
Significance Probable-Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene CCDC40
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000017.10:g.78073324A>G
CLNSRC
CLNACC RCV000204611.1,