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rs771663107

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771663107(A;A)
Make rs771663107(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position13865675
GeneDNAH5
is asnp
is mentioned by
dbSNPrs771663107
ebirs771663107
HLIrs771663107
Exacrs771663107
Varsomers771663107
Maprs771663107
PheGenIrs771663107
hapmaprs771663107
1000 genomesrs771663107
hgdprs771663107
ensemblrs771663107
gopubmedrs771663107
geneviewrs771663107
scholarrs771663107
googlers771663107
pharmgkbrs771663107
gwascentralrs771663107
openSNPrs771663107
23andMers771663107
23andMe allrs771663107
SNP Nexus

SNPshotrs771663107
SNPdbers771663107
MSV3drs771663107
GWAS Ctlgrs771663107
Max Magnitude0
ClinVar
Risk rs771663107(A;A)
Alt rs771663107(A;A)
Reference rs771663107(G;G)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene DNAH5
CLNDBN Kartagener syndrome
Reversed 0
HGVS NC_000005.9:g.13865784G>A
CLNSRC
CLNACC RCV000190910.1,