SNP Report

Basic Info

Name	rs3816448 dbSNP Ensembl
Location	chr2:174748331 - 174748331(1)
Variant Alleles	A/C/G
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.366613
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000409323); intron_variant(ENST00000261007, ENST00000348749, ENST00000409219, ENST00000409542, ENST00000435083, ENST00000442996, ENST00000636168); NMD_transcript_variant(ENST00000435083); non_coding_transcript_variant(ENST00000442996)
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)
CHRNA1	cholinergic receptor, nicotinic, alpha 1 (muscle)	2q31.1	2(0/1/1)

SNPs in LD with rs3816448 (count: 0) View in gBrowse (chr2:174748331..174748331 )

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

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