SNP Report

Basic Info

Name	rs965560 dbSNP Ensembl
Location	chr11:113201883 - 113201883(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.403954
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000316851, ENST00000401611, ENST00000525973, ENST00000529356, ENST00000531044, ENST00000611284, ENST00000613217, ENST00000615112, ENST00000615285, ENST00000618266, ENST00000619839, ENST00000620046, ENST00000621128, ENST00000621518, ENST00000621850); non_coding_transcript_variant(ENST00000525973, ENST00000611284)
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)
NCAM1	neural cell adhesion molecule 1	11q23.2	3(2/1/0)

SNPs in LD with rs965560 (count: 0) View in gBrowse (chr11:113201883..113201883 )

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

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