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rs72657393

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72657393(C;T)
Make rs72657393(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position21808041
GeneDNAH11
is asnp
is mentioned by
dbSNPrs72657393
ebirs72657393
HLIrs72657393
Exacrs72657393
Varsomers72657393
Maprs72657393
PheGenIrs72657393
hapmaprs72657393
1000 genomesrs72657393
hgdprs72657393
ensemblrs72657393
gopubmedrs72657393
geneviewrs72657393
scholarrs72657393
googlers72657393
pharmgkbrs72657393
gwascentralrs72657393
openSNPrs72657393
23andMers72657393
23andMe allrs72657393
SNP Nexus

SNPshotrs72657393
SNPdbers72657393
MSV3drs72657393
GWAS Ctlgrs72657393
Max Magnitude0
ClinVar
Risk rs72657393(T;T)
Alt rs72657393(T;T)
Reference rs72657393(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAH11
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000007.13:g.21847659C>T
CLNSRC
CLNACC RCV000228211.1,