Have questions? Visit https://www.reddit.com/r/SNPedia

rs797046109

From SNPedia

Orientationplus
Make rs797046109(-;-)
Make rs797046109(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position36102960
GeneWDR62
is asnp
is mentioned by
dbSNPrs797046109
ebirs797046109
HLIrs797046109
Exacrs797046109
Varsomers797046109
Maprs797046109
PheGenIrs797046109
hapmaprs797046109
1000 genomesrs797046109
hgdprs797046109
ensemblrs797046109
gopubmedrs797046109
geneviewrs797046109
scholarrs797046109
googlers797046109
pharmgkbrs797046109
gwascentralrs797046109
openSNPrs797046109
23andMers797046109
23andMe allrs797046109
SNP Nexus

SNPshotrs797046109
SNPdbers797046109
MSV3drs797046109
GWAS Ctlgrs797046109
Max Magnitude
ClinVar
Risk rs797046109(;)
Alt rs797046109(;)
Reference rs797046109(C;C)
Significance Probable-Pathogenic
Disease Primary autosomal recessive microcephaly 2
Variation info
Gene WDR62
CLNDBN Primary autosomal recessive microcephaly 2
Reversed 0
HGVS NC_000019.9:g.36593862delC
CLNSRC
CLNACC RCV000194814.1,