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rs869320712

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869320712(-;-)
Make rs869320712(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position84643719
GeneWDR73
is asnp
is mentioned by
dbSNPrs869320712
ebirs869320712
HLIrs869320712
Exacrs869320712
Varsomers869320712
Maprs869320712
PheGenIrs869320712
hapmaprs869320712
1000 genomesrs869320712
hgdprs869320712
ensemblrs869320712
gopubmedrs869320712
geneviewrs869320712
scholarrs869320712
googlers869320712
pharmgkbrs869320712
gwascentralrs869320712
openSNPrs869320712
23andMers869320712
23andMe allrs869320712
SNP Nexus

SNPshotrs869320712
SNPdbers869320712
MSV3drs869320712
GWAS Ctlgrs869320712
Max Magnitude0
ClinVar
Risk rs869320712(;)
Alt rs869320712(;)
Reference rs869320712(T;T)
Significance Pathogenic
Disease Microcephaly not provided
Variation info
Gene WDR73
CLNDBN Microcephaly, hiatal hernia and nephrotic syndrome not provided
Reversed 1
HGVS NC_000015.9:g.85186950delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000210866.1, RCV000224128.1,