SNP Report

Basic Info
Name rs383964 dbSNP Ensembl
Location chr22:18913156 - 18913156(1)
Variant Alleles A/C/G/T
Minor Allele A
Minor Allele Frequence 0.0924521
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000334029, ENST00000357068, ENST00000420436, ENST00000483718, ENST00000610940); downstream_gene_variant(ENST00000331444, ENST00000413981, ENST00000427407, ENST00000436645, ENST00000477156, ENST00000480608, ENST00000608842, ENST00000609229); NMD_transcript_variant(ENST00000483718); non_coding_transcript_exon_variant(ENST00000313755, ENST00000429300, ENST00000482858, ENST00000491604); non_coding_transcript_variant(ENST00000313755, ENST00000429300, ENST00000482858, ENST00000491604)
No. of Studies 1 (Positive: 1; Negative: 0; Trend: 0)
Source Literature
Overlap with SZ? NO
Overlap with MDD? NO

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Prata, D. P., 2006 no P-value no P-value A chi-square analysis showed no genotype-wise or allele-wise...... A chi-square analysis showed no genotype-wise or allele-wise association for any individual SNP. More... Positive

SNP related genes (count: 2)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
DGCR6 DiGeorge syndrome critical region gene 6 22q11.21 1(0/1/0)
PRODH proline dehydrogenase (oxidase) 1 22q11.2 4(0/4/0)

SNPs in LD with rs383964 (count: 0) View in gBrowse (chr22:18913156..18913156 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)