SNP Report

Basic Info

Name	rs4820379 dbSNP Ensembl
Location	chr22:39508608 - 39508608(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.378794
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000464629, ENST00000467866, ENST00000478342, ENST00000479514, ENST00000481746, ENST00000489792, ENST00000494219, ENST00000637854); intron_variant(ENST00000325301, ENST00000402881, ENST00000404569, ENST00000428069, ENST00000433117, ENST00000434364); NMD_transcript_variant(ENST00000428069, ENST00000433117)
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 rs4820379 (count: 0) View in gBrowse (chr22:39508608..39508608 )

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

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