SNP Report

Basic Info

Name	rs4409766 dbSNP Ensembl
Location	chr10:102856906 - 102856906(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.209864
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000299353, ENST00000339834, ENST00000369883, ENST00000478833); NMD_transcript_variant(ENST00000299353); non_coding_transcript_variant(ENST00000478833); upstream_gene_variant(ENST00000440461, ENST00000629474, ENST00000631443, ENST00000632794)
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)
C10orf32	chromosome 10 open reading frame 32	10q24.33	Mapped by LD-proxy

SNPs in LD with rs4409766 (count: 0) View in gBrowse (chr10:102856906..102856906 )

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

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