Have questions? Visit https://www.reddit.com/r/SNPedia

rs797045152

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045152(A;A)
Make rs797045152(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position55220382
GeneMCIDAS
is asnp
is mentioned by
dbSNPrs797045152
ebirs797045152
HLIrs797045152
Exacrs797045152
Varsomers797045152
Maprs797045152
PheGenIrs797045152
hapmaprs797045152
1000 genomesrs797045152
hgdprs797045152
ensemblrs797045152
gopubmedrs797045152
geneviewrs797045152
scholarrs797045152
googlers797045152
pharmgkbrs797045152
gwascentralrs797045152
openSNPrs797045152
23andMers797045152
23andMe allrs797045152
SNP Nexus

SNPshotrs797045152
SNPdbers797045152
MSV3drs797045152
GWAS Ctlgrs797045152
Max Magnitude0
ClinVar
Risk rs797045152(A;A)
Alt rs797045152(A;A)
Reference rs797045152(G;G)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene MCIDAS
CLNDBN Kartagener syndrome
Reversed 1
HGVS NC_000005.9:g.54516210C>T
CLNSRC
CLNACC RCV000190952.1,