SNP Report

Basic Info

Name	rs395440 dbSNP Ensembl
Location	chr22:18914365 - 18914365(1)
Variant Alleles	C/A/G
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.162141
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000331444, ENST00000413981, ENST00000427407, ENST00000436645, ENST00000477156, ENST00000480608, ENST00000483718, ENST00000609229); intron_variant(ENST00000313755, ENST00000334029, ENST00000357068, ENST00000420436, ENST00000429300, ENST00000482858, ENST00000491604, ENST00000610940); non_coding_transcript_variant(ENST00000313755, ENST00000429300, ENST00000482858, ENST00000491604)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

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 rs395440 (count: 0) View in gBrowse (chr22:18914365..18914365 )

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

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