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rs730882206

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882206(A;A)
Make rs730882206(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position1725804
GeneWDR81
is asnp
is mentioned by
dbSNPrs730882206
ebirs730882206
HLIrs730882206
Exacrs730882206
Varsomers730882206
Maprs730882206
PheGenIrs730882206
hapmaprs730882206
1000 genomesrs730882206
hgdprs730882206
ensemblrs730882206
gopubmedrs730882206
geneviewrs730882206
scholarrs730882206
googlers730882206
pharmgkbrs730882206
gwascentralrs730882206
openSNPrs730882206
23andMers730882206
23andMe allrs730882206
SNP Nexus

SNPshotrs730882206
SNPdbers730882206
MSV3drs730882206
GWAS Ctlgrs730882206
Max Magnitude0
ClinVar
Risk rs730882206(A;A)
Alt rs730882206(A;A)
Reference rs730882206(G;G)
Significance Probable-Pathogenic
Disease Hydranencephaly Neonatal death Severe brain malformation Severe cerebellar hypoplasia not provided
Variation info
Gene WDR81
CLNDBN Hydranencephaly Neonatal death Severe brain malformation Severe cerebellar hypoplasia not provided
Reversed 0
HGVS NC_000017.10:g.1629098G>A
CLNSRC
CLNACC RCV000162111.1, RCV000171248.1,