SNP Report

Basic Info

Name	rs5758092 dbSNP Ensembl
Location	chr22:40819179 - 40819179(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.152556
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000263255, ENST00000412879, ENST00000420970, ENST00000426396, ENST00000427084, ENST00000430221, ENST00000434185, ENST00000434193, ENST00000435456, ENST00000443810, ENST00000447566, ENST00000449676, ENST00000458600, ENST00000491545, ENST00000544408); NMD_transcript_variant(ENST00000263255, ENST00000412879, ENST00000420970, ENST00000426396, ENST00000427084, ENST00000430221, ENST00000434193, ENST00000443810, ENST00000447566, ENST00000449676, ENST00000458600); non_coding_transcript_variant(ENST00000491545)
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)
SLC25A17	solute carrier family 25 (mitochondrial carrier; peroxisomal membrane protein, 34kDa), member 17	22q13.2	Mapped by LD-proxy

SNPs in LD with rs5758092 (count: 0) View in gBrowse (chr22:40819179..40819179 )

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

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