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rs754099015

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754099015(A;A)
Make rs754099015(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position84643568
GeneWDR73
is asnp
is mentioned by
dbSNPrs754099015
ebirs754099015
HLIrs754099015
Exacrs754099015
Varsomers754099015
Maprs754099015
PheGenIrs754099015
hapmaprs754099015
1000 genomesrs754099015
hgdprs754099015
ensemblrs754099015
gopubmedrs754099015
geneviewrs754099015
scholarrs754099015
googlers754099015
pharmgkbrs754099015
gwascentralrs754099015
openSNPrs754099015
23andMers754099015
23andMe allrs754099015
SNP Nexus

SNPshotrs754099015
SNPdbers754099015
MSV3drs754099015
GWAS Ctlgrs754099015
Max Magnitude0
ClinVar
Risk rs754099015(A;A)
Alt rs754099015(A;A)
Reference rs754099015(G;G)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene WDR73
CLNDBN Microcephaly, hiatal hernia and nephrotic syndrome
Reversed 0
HGVS NC_000015.9:g.85186799G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190490.3,