SNP Report

Basic Info

Name	rs11647738 dbSNP Ensembl
Location	chr16:65022047 - 65022047(1)
Variant Alleles	C/A
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.0908546
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000268603, ENST00000394156, ENST00000562325, ENST00000562712, ENST00000562882, ENST00000562998, ENST00000564317, ENST00000565210, ENST00000566827, ENST00000567934, ENST00000568340, ENST00000569624); non_coding_transcript_variant(ENST00000565210, ENST00000568340, ENST00000569624)
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)
CDH11	cadherin 11, type 2, OB-cadherin (osteoblast)	16q21	Mapped by LD-proxy

SNPs in LD with rs11647738 (count: 0) View in gBrowse (chr16:65022047..65022047 )

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

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