SNP Report

Basic Info

Name	rs6977512 dbSNP Ensembl
Location	chr7:39465460 - 39465460(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.470647
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000518318); downstream_gene_variant(ENST00000403058, ENST00000416452, ENST00000559001); intron_variant(ENST00000426456); non_coding_transcript_variant(ENST00000426456)
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)
POU6F2	POU class 6 homeobox 2	7p14.1	1(1/0/0)

SNPs in LD with rs6977512 (count: 0) View in gBrowse (chr7:39465460..39465460 )

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

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