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rs797044994

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044994(C;T)
Make rs797044994(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position84643667
GeneWDR73
is asnp
is mentioned by
dbSNPrs797044994
ebirs797044994
HLIrs797044994
Exacrs797044994
Varsomers797044994
Maprs797044994
PheGenIrs797044994
hapmaprs797044994
1000 genomesrs797044994
hgdprs797044994
ensemblrs797044994
gopubmedrs797044994
geneviewrs797044994
scholarrs797044994
googlers797044994
pharmgkbrs797044994
gwascentralrs797044994
openSNPrs797044994
23andMers797044994
23andMe allrs797044994
SNP Nexus

SNPshotrs797044994
SNPdbers797044994
MSV3drs797044994
GWAS Ctlgrs797044994
Max Magnitude0
ClinVar
Risk rs797044994(T;T)
Alt rs797044994(T;T)
Reference rs797044994(C;C)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene WDR73
CLNDBN Microcephaly, hiatal hernia and nephrotic syndrome
Reversed 1
HGVS NC_000015.9:g.85186898G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190492.3,