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rs767086146

From SNPedia

Orientationplus
Make rs767086146(-;-)
Make rs767086146(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position84646300
GeneWDR73
is asnp
is mentioned by
dbSNPrs767086146
ebirs767086146
HLIrs767086146
Exacrs767086146
Varsomers767086146
Maprs767086146
PheGenIrs767086146
hapmaprs767086146
1000 genomesrs767086146
hgdprs767086146
ensemblrs767086146
gopubmedrs767086146
geneviewrs767086146
scholarrs767086146
googlers767086146
pharmgkbrs767086146
gwascentralrs767086146
openSNPrs767086146
23andMers767086146
23andMe allrs767086146
SNP Nexus

SNPshotrs767086146
SNPdbers767086146
MSV3drs767086146
GWAS Ctlgrs767086146
Max Magnitude
ClinVar
Risk rs767086146(;)
Alt rs767086146(;)
Reference rs767086146(CT;CT)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene WDR73
CLNDBN Microcephaly, hiatal hernia and nephrotic syndrome
Reversed 0
HGVS NC_000015.9:g.85189531_85189532delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000190489.2,