SNP Report

Basic Info

Name	rs310758 dbSNP Ensembl
Location	chr3:12177023 - 12177023(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.394768
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000425297, ENST00000439861, ENST00000620175, ENST00000621198); NMD_transcript_variant(ENST00000425297); non_coding_transcript_variant(ENST00000439861)
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)
SYN2	synapsin II	3p25.2	1(0/1/0)

SNPs in LD with rs310758 (count: 0) View in gBrowse (chr3:12177023..12177023 )

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

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