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rs397515565

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515565(C;C)
Make rs397515565(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position74310164
GeneDNAI2
is asnp
is mentioned by
dbSNPrs397515565
ebirs397515565
HLIrs397515565
Exacrs397515565
Varsomers397515565
Maprs397515565
PheGenIrs397515565
hapmaprs397515565
1000 genomesrs397515565
hgdprs397515565
ensemblrs397515565
gopubmedrs397515565
geneviewrs397515565
scholarrs397515565
googlers397515565
pharmgkbrs397515565
gwascentralrs397515565
openSNPrs397515565
23andMers397515565
23andMe allrs397515565
SNP Nexus

SNPshotrs397515565
SNPdbers397515565
MSV3drs397515565
GWAS Ctlgrs397515565
Max Magnitude0
ClinVar
Risk rs397515565(C,T;C,T)
Alt rs397515565(C,T;C,T)
Reference rs397515565(G;G)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene DNAI2
CLNDBN Kartagener syndrome
Reversed 0
HGVS NC_000017.10:g.72306303G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000055951.2,