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

rs1085308033

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome1
Position151018494
GenePRUNE, PRUNE1
is asnp
is mentioned by
dbSNPrs1085308033
dbSNP (old)rs1085308033
ClinGenrs1085308033
ebirs1085308033
HLIrs1085308033
Exacrs1085308033
Gnomadrs1085308033
Varsomers1085308033
Maprs1085308033
PheGenIrs1085308033
Biobankrs1085308033
1000 genomesrs1085308033
hgdprs1085308033
ensemblrs1085308033
gopubmedrs1085308033
geneviewrs1085308033
scholarrs1085308033
googlers1085308033
pharmgkbrs1085308033
gwascentralrs1085308033
openSNPrs1085308033
23andMers1085308033
23andMe allrs1085308033
SNPshotrs1085308033
SNPdbers1085308033
MSV3drs1085308033
GWAS Ctlgrs1085308033
Max Magnitude0
ClinVar
Risk rs1085308033(A;A)
Alt rs1085308033(A;A)
Reference Rs1085308033(C;C)
Significance Pathogenic
Disease Neurodevelopmental disorder with microcephaly
Variation info
Gene PRUNE PRUNE1
CLNDBN Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies
Reversed 0
HGVS NC_000001.10:g.150990970C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000490539.1,