SNP Report

Basic Info

Name	rs9679638 dbSNP Ensembl
Location	chr2:100977992 - 100977992(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.246206
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000335681, ENST00000450763, ENST00000471974, ENST00000474550); non_coding_transcript_variant(ENST00000471974, ENST00000474550); upstream_gene_variant(ENST00000433012, ENST00000433408, ENST00000439150, ENST00000446644)
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)
NPAS2	neuronal PAS domain protein 2	2q11.2	5(3/2/0)

SNPs in LD with rs9679638 (count: 0) View in gBrowse (chr2:100977992..100977992 )

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

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