SNP Report

Basic Info

Name	rs2294360 dbSNP Ensembl
Location	chr22:39501787 - 39501787(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.430112
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000402881, ENST00000464629, ENST00000467866); non_coding_transcript_exon_variant(ENST00000465564); non_coding_transcript_variant(ENST00000464629, ENST00000465564, ENST00000467866); upstream_gene_variant(ENST00000325301, ENST00000404569, ENST00000428069, ENST00000433117, ENST00000434364, ENST00000478342, ENST00000479514, ENST00000481746, ENST00000489792, ENST00000494219, ENST00000637854)
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)
SMCR7L	mitochondrial elongation factor 1	22q13.1	Mapped by LD-proxy

SNPs in LD with rs2294360 (count: 0) View in gBrowse (chr22:39501787..39501787 )

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

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