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rs2073738

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2073738(A;A)
Make rs2073738(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19183443
GeneCLTCL1
is asnp
is mentioned by
dbSNPrs2073738
ebirs2073738
HLIrs2073738
Exacrs2073738
Varsomers2073738
Maprs2073738
PheGenIrs2073738
hapmaprs2073738
1000 genomesrs2073738
hgdprs2073738
ensemblrs2073738
gopubmedrs2073738
geneviewrs2073738
scholarrs2073738
googlers2073738
pharmgkbrs2073738
gwascentralrs2073738
openSNPrs2073738
23andMers2073738
23andMe allrs2073738
SNP Nexus

SNPshotrs2073738
SNPdbers2073738
MSV3drs2073738
GWAS Ctlgrs2073738
GMAF0.008264
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 22511880OA-icon.png] Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism


GET Evidence
CLTCL1-V1591L
aa_change Val1591Leu
aa_change_short V1591L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.015625
summary