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rs757013900

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs757013900(C;T)
Make rs757013900(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position21635991
GeneDNAH11
is asnp
is mentioned by
dbSNPrs757013900
ebirs757013900
HLIrs757013900
Exacrs757013900
Varsomers757013900
Maprs757013900
PheGenIrs757013900
hapmaprs757013900
1000 genomesrs757013900
hgdprs757013900
ensemblrs757013900
gopubmedrs757013900
geneviewrs757013900
scholarrs757013900
googlers757013900
pharmgkbrs757013900
gwascentralrs757013900
openSNPrs757013900
23andMers757013900
23andMe allrs757013900
SNP Nexus

SNPshotrs757013900
SNPdbers757013900
MSV3drs757013900
GWAS Ctlgrs757013900
Max Magnitude0
ClinVar
Risk rs757013900(T;T)
Alt rs757013900(T;T)
Reference rs757013900(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAH11
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000007.13:g.21675609C>T
CLNSRC
CLNACC RCV000232517.1,