SNP Report

Basic Info

Name	rs1120755 dbSNP Ensembl
Location	chr2:107527011 - 107527011(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele Frequence	0.0
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000414300); non_coding_transcript_variant(ENST00000414300); upstream_gene_variant(ENST00000443205)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs1120755 (count: 0) View in gBrowse (chr2:107527011..107527011 )

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

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