SNP Report

Basic Info

Name	rs7674000 dbSNP Ensembl
Location	chr4:52691511 - 52691511(1)
Variant Alleles	C/A
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.120208
Functional Annotation	non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	non_coding_transcript_exon_variant(ENST00000564513); non_coding_transcript_variant(ENST00000564513)
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 rs7674000 (count: 0) View in gBrowse (chr4:52691511..52691511 )

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

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