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rs727502864

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs727502864(-;-)
Make rs727502864(-;C)
Make rs727502864(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position84645587
GeneWDR73
is asnp
is mentioned by
dbSNPrs727502864
ebirs727502864
HLIrs727502864
Exacrs727502864
Varsomers727502864
Maprs727502864
PheGenIrs727502864
hapmaprs727502864
1000 genomesrs727502864
hgdprs727502864
ensemblrs727502864
gopubmedrs727502864
geneviewrs727502864
scholarrs727502864
googlers727502864
pharmgkbrs727502864
gwascentralrs727502864
openSNPrs727502864
23andMers727502864
23andMe allrs727502864
SNP Nexus

SNPshotrs727502864
SNPdbers727502864
MSV3drs727502864
GWAS Ctlgrs727502864
Max Magnitude0
ClinVar
Risk rs727502864(C;C)
Alt rs727502864(C;C)
Reference rs727502864(;)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene WDR73
CLNDBN Microcephaly, hiatal hernia and nephrotic syndrome
Reversed 1
HGVS NC_000015.9:g.85188819dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000150039.2,