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

rs587783390

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783390(C;T)
Make rs587783390(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position120409290
GeneCDK5RAP2
is asnp
is mentioned by
dbSNPrs587783390
ebirs587783390
HLIrs587783390
Exacrs587783390
Varsomers587783390
Maprs587783390
PheGenIrs587783390
hapmaprs587783390
1000 genomesrs587783390
hgdprs587783390
ensemblrs587783390
gopubmedrs587783390
geneviewrs587783390
scholarrs587783390
googlers587783390
pharmgkbrs587783390
gwascentralrs587783390
openSNPrs587783390
23andMers587783390
23andMe allrs587783390
SNP Nexus

SNPshotrs587783390
SNPdbers587783390
MSV3drs587783390
GWAS Ctlgrs587783390
Max Magnitude0
ClinVar
Risk rs587783390(T;T)
Alt rs587783390(T;T)
Reference rs587783390(C;C)
Significance Other
Disease Primary autosomal recessive microcephaly 3
Variation info
Gene CDK5RAP2
CLNDBN Primary autosomal recessive microcephaly 3
Reversed 1
HGVS NC_000009.11:g.123171568G>A
CLNSRC
CLNACC RCV000145486.2,