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rs745800041

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745800041(C;T)
Make rs745800041(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position19482803
GeneCDC45
is asnp
is mentioned by
dbSNPrs745800041
ebirs745800041
HLIrs745800041
Exacrs745800041
Varsomers745800041
Maprs745800041
PheGenIrs745800041
hapmaprs745800041
1000 genomesrs745800041
hgdprs745800041
ensemblrs745800041
gopubmedrs745800041
geneviewrs745800041
scholarrs745800041
googlers745800041
pharmgkbrs745800041
gwascentralrs745800041
openSNPrs745800041
23andMers745800041
23andMe allrs745800041
SNP Nexus

SNPshotrs745800041
SNPdbers745800041
MSV3drs745800041
GWAS Ctlgrs745800041
Max Magnitude0
ClinVar
Risk rs745800041(T;T)
Alt rs745800041(T;T)
Reference rs745800041(C;C)
Significance Pathogenic
Disease Meier-gorlin syndrome 7
Variation info
Gene CDC45
CLNDBN Meier-gorlin syndrome 7
Reversed 0
HGVS NC_000022.10:g.19470326C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000239576.1,