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rs754080445

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs754080445(A;G)
Make rs754080445(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position19499124
GeneCDC45
is asnp
is mentioned by
dbSNPrs754080445
ebirs754080445
HLIrs754080445
Exacrs754080445
Varsomers754080445
Maprs754080445
PheGenIrs754080445
hapmaprs754080445
1000 genomesrs754080445
hgdprs754080445
ensemblrs754080445
gopubmedrs754080445
geneviewrs754080445
scholarrs754080445
googlers754080445
pharmgkbrs754080445
gwascentralrs754080445
openSNPrs754080445
23andMers754080445
23andMe allrs754080445
SNP Nexus

SNPshotrs754080445
SNPdbers754080445
MSV3drs754080445
GWAS Ctlgrs754080445
Max Magnitude0
ClinVar
Risk rs754080445(G;G)
Alt rs754080445(G;G)
Reference rs754080445(A;A)
Significance Pathogenic
Disease Meier-gorlin syndrome 7
Variation info
Gene CDC45
CLNDBN Meier-gorlin syndrome 7
Reversed 0
HGVS NC_000022.10:g.19486647A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000239518.1,