SNP Report

Basic Info

Name	rs12586996 dbSNP Ensembl
Location	chr14:73342516 - 73342516(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.315495
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000355058, ENST00000356296, ENST00000359560, ENST00000535282, ENST00000544991, ENST00000554315, ENST00000554394, ENST00000554521, ENST00000554546, ENST00000554818, ENST00000555238, ENST00000555307, ENST00000555394, ENST00000555738, ENST00000555859, ENST00000555987, ENST00000556112, ENST00000557597, ENST00000557774, ENST00000559312, ENST00000560335); non_coding_transcript_variant(ENST00000554315, ENST00000556112, ENST00000557774)
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)
NUMB	numb homolog (Drosophila)	14q24.3	1(0/0/1)

SNPs in LD with rs12586996 (count: 0) View in gBrowse (chr14:73342516..73342516 )

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

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