SNP Report

Basic Info

Name	rs4677841 dbSNP Ensembl
Location	chr3:195411699 - 195411699(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.452875
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000326793, ENST00000439666, ENST00000447662, ENST00000480906, ENST00000481463, ENST00000618471, ENST00000635383); NMD_transcript_variant(ENST00000447662); non_coding_transcript_variant(ENST00000480906, ENST00000481463)
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)
ACAP2	ArfGAP with coiled-coil, ankyrin repeat and PH domains 2	3q29	1(0/1/0)

SNPs in LD with rs4677841 (count: 0) View in gBrowse (chr3:195411699..195411699 )

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

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