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rs797044993

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044993(A;A)
Make rs797044993(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position84653673
GeneWDR73
is asnp
is mentioned by
dbSNPrs797044993
ebirs797044993
HLIrs797044993
Exacrs797044993
Varsomers797044993
Maprs797044993
PheGenIrs797044993
hapmaprs797044993
1000 genomesrs797044993
hgdprs797044993
ensemblrs797044993
gopubmedrs797044993
geneviewrs797044993
scholarrs797044993
googlers797044993
pharmgkbrs797044993
gwascentralrs797044993
openSNPrs797044993
23andMers797044993
23andMe allrs797044993
SNP Nexus

SNPshotrs797044993
SNPdbers797044993
MSV3drs797044993
GWAS Ctlgrs797044993
Max Magnitude0
ClinVar
Risk rs797044993(A;A)
Alt rs797044993(A;A)
Reference rs797044993(T;T)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene WDR73
CLNDBN Microcephaly, hiatal hernia and nephrotic syndrome
Reversed 1
HGVS NC_000015.9:g.85196904A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190491.2,