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rs777031813

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777031813(G;T)
Make rs777031813(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position55222341
GeneMCIDAS
is asnp
is mentioned by
dbSNPrs777031813
ebirs777031813
HLIrs777031813
Exacrs777031813
Varsomers777031813
Maprs777031813
PheGenIrs777031813
hapmaprs777031813
1000 genomesrs777031813
hgdprs777031813
ensemblrs777031813
gopubmedrs777031813
geneviewrs777031813
scholarrs777031813
googlers777031813
pharmgkbrs777031813
gwascentralrs777031813
openSNPrs777031813
23andMers777031813
23andMe allrs777031813
SNP Nexus

SNPshotrs777031813
SNPdbers777031813
MSV3drs777031813
GWAS Ctlgrs777031813
Max Magnitude0
ClinVar
Risk rs777031813(T;T)
Alt rs777031813(T;T)
Reference rs777031813(G;G)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene MCIDAS
CLNDBN Kartagener syndrome
Reversed 0
HGVS NC_000005.9:g.54518169G>T
CLNSRC
CLNACC RCV000190950.1,