SNP Report

Basic Info

Name	rs7373977 dbSNP Ensembl
Location	chr3:197989109 - 197989109(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.389976
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000330198, ENST00000332636, ENST00000420910, ENST00000451139, ENST00000472063, ENST00000473676, ENST00000476356, ENST00000482695); non_coding_transcript_variant(ENST00000451139, ENST00000472063, ENST00000473676, ENST00000476356); upstream_gene_variant(ENST00000480813)
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)
LMLN	leishmanolysin-like (metallopeptidase M8 family)	3q29	1(0/1/0)

SNPs in LD with rs7373977 (count: 0) View in gBrowse (chr3:197989109..197989109 )

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

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