SNP Report

Basic Info

Name	rs885071 dbSNP Ensembl
Location	chrCHR_HSCHR15_4_CTG8:32183206 - 32183206(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.344848
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000306901, ENST00000437966, ENST00000454250, ENST00000635722, ENST00000635759, ENST00000635884, ENST00000635978, ENST00000636044, ENST00000636271, ENST00000636295, ENST00000636440, ENST00000636603, ENST00000636647, ENST00000636850, ENST00000637033, ENST00000637183, ENST00000637350, ENST00000637519, ENST00000637552, ENST00000637786, ENST00000637971, ENST00000638031, ENST00000638106); NMD_transcript_variant(ENST00000437966, ENST00000635722, ENST00000635759, ENST00000636044, ENST00000636271, ENST00000636850, ENST00000637350, ENST00000637519, ENST00000637786, ENST00000637971, ENST00000638031); non_coding_transcript_variant(ENST00000636295, ENST00000636647, ENST00000455693)
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)
CHRNA7	cholinergic receptor, nicotinic, alpha 7 (neuronal)	15q13.3	4(2/2/0)

SNPs in LD with rs885071 (count: 0) View in gBrowse (chrCHR_HSCHR15_4_CTG8:32183206..32183206 )

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

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