SNP Report

Basic Info

Name	rs17207897 dbSNP Ensembl
Location	chr10:60057722 - 60057722(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.0307508
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000459732, ENST00000511043, ENST00000514197, ENST00000613207); intron_variant(ENST00000280772, ENST00000355288, ENST00000373820, ENST00000373827, ENST00000414383, ENST00000469721, ENST00000503366, ENST00000610321, ENST00000610901, ENST00000612776, ENST00000616444, ENST00000619719); non_coding_transcript_variant(ENST00000414383, ENST00000469721, ENST00000619719); upstream_gene_variant(ENST00000502769, ENST00000617800)
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)
ANK3	ankyrin 3, node of Ranvier (ankyrin G)	10q21	17(13/3/1)

SNPs in LD with rs17207897 (count: 0) View in gBrowse (chr10:60057722..60057722 )

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

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