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rs72657321

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72657321(C;T)
Make rs72657321(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position21620016
GeneDNAH11
is asnp
is mentioned by
dbSNPrs72657321
ebirs72657321
HLIrs72657321
Exacrs72657321
Varsomers72657321
Maprs72657321
PheGenIrs72657321
hapmaprs72657321
1000 genomesrs72657321
hgdprs72657321
ensemblrs72657321
gopubmedrs72657321
geneviewrs72657321
scholarrs72657321
googlers72657321
pharmgkbrs72657321
gwascentralrs72657321
openSNPrs72657321
23andMers72657321
23andMe allrs72657321
SNP Nexus

SNPshotrs72657321
SNPdbers72657321
MSV3drs72657321
GWAS Ctlgrs72657321
Max Magnitude0
ClinVar
Risk rs72657321(T;T)
Alt rs72657321(T;T)
Reference rs72657321(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAH11
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000007.13:g.21659634C>T
CLNSRC
CLNACC RCV000230700.1,