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rs730882204

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730882204(C;C)
Make rs730882204(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position89702026
GeneWDR93
is asnp
is mentioned by
dbSNPrs730882204
ebirs730882204
HLIrs730882204
Exacrs730882204
Varsomers730882204
Maprs730882204
PheGenIrs730882204
hapmaprs730882204
1000 genomesrs730882204
hgdprs730882204
ensemblrs730882204
gopubmedrs730882204
geneviewrs730882204
scholarrs730882204
googlers730882204
pharmgkbrs730882204
gwascentralrs730882204
openSNPrs730882204
23andMers730882204
23andMe allrs730882204
SNP Nexus

SNPshotrs730882204
SNPdbers730882204
MSV3drs730882204
GWAS Ctlgrs730882204
Max Magnitude0
ClinVar
Risk rs730882204(C;C)
Alt rs730882204(C;C)
Reference rs730882204(T;T)
Significance Probable-Pathogenic
Disease Autistic spectrum disorder with isolated skills
Variation info
Gene WDR93
CLNDBN Autistic spectrum disorder with isolated skills
Reversed 0
HGVS NC_000015.9:g.90245257T>C
CLNSRC
CLNACC RCV000162108.1,