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rs797045148

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045148(A;A)
Make rs797045148(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position42485804
GeneRSPH1
is asnp
is mentioned by
dbSNPrs797045148
ebirs797045148
HLIrs797045148
Exacrs797045148
Varsomers797045148
Maprs797045148
PheGenIrs797045148
hapmaprs797045148
1000 genomesrs797045148
hgdprs797045148
ensemblrs797045148
gopubmedrs797045148
geneviewrs797045148
scholarrs797045148
googlers797045148
pharmgkbrs797045148
gwascentralrs797045148
openSNPrs797045148
23andMers797045148
23andMe allrs797045148
SNP Nexus

SNPshotrs797045148
SNPdbers797045148
MSV3drs797045148
GWAS Ctlgrs797045148
Max Magnitude0
ClinVar
Risk rs797045148(A;A)
Alt rs797045148(A;A)
Reference rs797045148(G;G)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene RSPH1
CLNDBN Kartagener syndrome
Reversed 1
HGVS NC_000021.8:g.43905914C>T
CLNSRC
CLNACC RCV000190925.1,