SNP Report

Basic Info

Name	rs3960073 dbSNP Ensembl
Location	chr22:18920904 - 18920904(1)
Variant Alleles	T/C
Minor Allele	T
Minor Allele Frequence	0.303914
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000399694, ENST00000438924, ENST00000450579, ENST00000457083, ENST00000496625); intron_variant(ENST00000334029, ENST00000357068, ENST00000420436, ENST00000429300, ENST00000446371, ENST00000491604, ENST00000610940); non_coding_transcript_exon_variant(ENST00000313755, ENST00000482858, ENST00000609229); non_coding_transcript_variant(ENST00000313755, ENST00000429300, ENST00000446371, ENST00000482858, ENST00000491604, ENST00000609229)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
PRODH	proline dehydrogenase (oxidase) 1	22q11.2	4(0/4/0)

SNPs in LD with rs3960073 (count: 0) View in gBrowse (chr22:18920904..18920904 )

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

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