SNP Report

Basic Info

Name	rs4643402 dbSNP Ensembl
Location	chr18:12056851 - 12056851(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.433506
Functional Annotation	non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	non_coding_transcript_exon_variant(ENST00000391405); non_coding_transcript_variant(ENST00000391405)
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 rs4643402 (count: 0) View in gBrowse (chr18:12056851..12056851 )

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

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