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rs147875659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147875659(A;A)
Make rs147875659(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position36084678
GeneWDR62
is asnp
is mentioned by
dbSNPrs147875659
ClinGenrs147875659
ebirs147875659
HLIrs147875659
Exacrs147875659
Varsomers147875659
Maprs147875659
PheGenIrs147875659
hapmaprs147875659
1000 genomesrs147875659
hgdprs147875659
ensemblrs147875659
gopubmedrs147875659
geneviewrs147875659
scholarrs147875659
googlers147875659
pharmgkbrs147875659
gwascentralrs147875659
openSNPrs147875659
23andMers147875659
23andMe allrs147875659
SNP Nexus

SNPshotrs147875659
SNPdbers147875659
MSV3drs147875659
GWAS Ctlgrs147875659
Max Magnitude0
ClinVar
Risk rs147875659(A;A)
Alt rs147875659(A;A)
Reference Rs147875659(G;G)
Significance Other
Disease Primary autosomal recessive microcephaly 2 not specified not provided
Variation info
Gene WDR62
CLNDBN Primary autosomal recessive microcephaly 2 not specified not provided
Reversed 0
HGVS NC_000019.9:g.36575580G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000000058.5, RCV000174280.1, RCV000489330.1,