SNP Report

Basic Info

Name	rs7684126 dbSNP Ensembl
Location	chr4:186151229 - 186151229(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.166733
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000508379); intron_variant(ENST00000227065, ENST00000356371, ENST00000389354, ENST00000502970, ENST00000503432, ENST00000504330, ENST00000509574, ENST00000510790, ENST00000513030, ENST00000513212, ENST00000514153, ENST00000514829, ENST00000515078); non_coding_transcript_variant(ENST00000513030, ENST00000513212, ENST00000514829, ENST00000515078)
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)
FAM149A	family with sequence similarity 149, member A	4q35.1	1(0/1/0)

SNPs in LD with rs7684126 (count: 0) View in gBrowse (chr4:186151229..186151229 )

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

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