SNP Report

Basic Info

Name	rs5758108 dbSNP Ensembl
Location	chr22:40854435 - 40854435(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.0858626
Functional Annotation	intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000216218, ENST00000411695, ENST00000455824, ENST00000620312); NMD_transcript_variant(ENST00000455824); upstream_gene_variant(ENST00000357137, ENST00000417688, ENST00000428799, ENST00000482652, ENST00000614001)
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)
XPNPEP3	X-prolyl aminopeptidase 3, mitochondrial	22q13.2	Mapped by LD-proxy
ST13	suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein)	22q13.2	1(1/0/0)

SNPs in LD with rs5758108 (count: 0) View in gBrowse (chr22:40854435..40854435 )

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

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