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rs797044992

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044992(C;T)
Make rs797044992(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position84645651
GeneWDR73
is asnp
is mentioned by
dbSNPrs797044992
ebirs797044992
HLIrs797044992
Exacrs797044992
Varsomers797044992
Maprs797044992
PheGenIrs797044992
hapmaprs797044992
1000 genomesrs797044992
hgdprs797044992
ensemblrs797044992
gopubmedrs797044992
geneviewrs797044992
scholarrs797044992
googlers797044992
pharmgkbrs797044992
gwascentralrs797044992
openSNPrs797044992
23andMers797044992
23andMe allrs797044992
SNP Nexus

SNPshotrs797044992
SNPdbers797044992
MSV3drs797044992
GWAS Ctlgrs797044992
Max Magnitude0
ClinVar
Risk rs797044992(T;T)
Alt rs797044992(T;T)
Reference rs797044992(C;C)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene WDR73
CLNDBN Microcephaly, hiatal hernia and nephrotic syndrome
Reversed 1
HGVS NC_000015.9:g.85188882G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190488.2,