SNP Report

Basic Info

Name	rs11662763 dbSNP Ensembl
Location	chr18:5857092 - 5857092(1)
Variant Alleles	C/T
Ancestral Allele	A
Minor Allele	T
Minor Allele Frequence	0.119609
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000562452); non_coding_transcript_variant(ENST00000562452)
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 rs11662763 (count: 0) View in gBrowse (chr18:5857092..5857092 )

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

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