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rs863223322

From SNPedia

Orientationplus
Make rs863223322(-;-)
Make rs863223322(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position36091251
GeneWDR62
is asnp
is mentioned by
dbSNPrs863223322
ebirs863223322
HLIrs863223322
Exacrs863223322
Varsomers863223322
Maprs863223322
PheGenIrs863223322
hapmaprs863223322
1000 genomesrs863223322
hgdprs863223322
ensemblrs863223322
gopubmedrs863223322
geneviewrs863223322
scholarrs863223322
googlers863223322
pharmgkbrs863223322
gwascentralrs863223322
openSNPrs863223322
23andMers863223322
23andMe allrs863223322
SNP Nexus

SNPshotrs863223322
SNPdbers863223322
MSV3drs863223322
GWAS Ctlgrs863223322
Max Magnitude
ClinVar
Risk rs863223322(;)
Alt rs863223322(;)
Reference rs863223322(A;A)
Significance Pathogenic
Disease Primary autosomal recessive microcephaly 2
Variation info
Gene WDR62
CLNDBN Primary autosomal recessive microcephaly 2
Reversed 0
HGVS NC_000019.9:g.36582153delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000024035.4,