SNP Report

Basic Info

Name	rs787884 dbSNP Ensembl
Location	chr9:132449252 - 132449252(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.448482
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000343036, ENST00000393215, ENST00000393216)
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)
C9orf171	chromosome 9 open reading frame 171	9q34.13	1(0/1/0)

SNPs in LD with rs787884 (count: 0) View in gBrowse (chr9:132449252..132449252 )

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

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