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rs727502863

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727502863(G;G)
Make rs727502863(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position84652783
GeneWDR73
is asnp
is mentioned by
dbSNPrs727502863
ebirs727502863
HLIrs727502863
Exacrs727502863
Varsomers727502863
Maprs727502863
PheGenIrs727502863
hapmaprs727502863
1000 genomesrs727502863
hgdprs727502863
ensemblrs727502863
gopubmedrs727502863
geneviewrs727502863
scholarrs727502863
googlers727502863
pharmgkbrs727502863
gwascentralrs727502863
openSNPrs727502863
23andMers727502863
23andMe allrs727502863
SNP Nexus

SNPshotrs727502863
SNPdbers727502863
MSV3drs727502863
GWAS Ctlgrs727502863
Max Magnitude0
ClinVar
Risk rs727502863(G;G)
Alt rs727502863(G;G)
Reference rs727502863(T;T)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene WDR73
CLNDBN Microcephaly, hiatal hernia and nephrotic syndrome
Reversed 1
HGVS NC_000015.9:g.85196014A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000150038.3,