SNP Report

Basic Info

Name	rs16961286 dbSNP Ensembl
Location	chr15:48638674 - 48638674(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.168331
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000558230, ENST00000560355); intron_variant(ENST00000316623, ENST00000537463, LRG_778t1); NMD_transcript_variant(ENST00000537463)
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)
FBN1	fibrillin 1	15q21.1	2(0/2/0)

SNPs in LD with rs16961286 (count: 0) View in gBrowse (chr15:48638674..48638674 )

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

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