SNP Report

Basic Info

Name	rs7973796 dbSNP Ensembl
Location	chr12:102202345 - 102202345(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.4377
Functional Annotation	downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000327680, ENST00000412715, ENST00000417507, ENST00000457614, ENST00000535811); non_coding_transcript_exon_variant(ENST00000626826); non_coding_transcript_variant(ENST00000626826); upstream_gene_variant(ENST00000329406)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
PMCH	pro-melanin-concentrating hormone	12q23.2	1(1/0/0)
PARPBP	PARP1 binding protein	12q23.2	Mapped by LD-proxy

SNPs in LD with rs7973796 (count: 0) View in gBrowse (chr12:102202345..102202345 )

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

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