SNP Report

Basic Info

Name	rs902909 dbSNP Ensembl
Location	chr4:188100311 - 188100311(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.289137
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000326754, ENST00000503141, ENST00000503475, ENST00000511771, ENST00000512729); NMD_transcript_variant(ENST00000503141, ENST00000503475); non_coding_transcript_variant(ENST00000511771)
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)
TRIML2	tripartite motif family-like 2	4q35.2	1(0/1/0)

SNPs in LD with rs902909 (count: 0) View in gBrowse (chr4:188100311..188100311 )

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

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