SNP Report

Basic Info

Name	rs4663865 dbSNP Ensembl
Location	chr2:238237319 - 238237319(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.0928514
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000272937, ENST00000409002, ENST00000409160, ENST00000409182, ENST00000409356, ENST00000409574, ENST00000417803, ENST00000436051, ENST00000438457, ENST00000450098); intron_variant(ENST00000456601); non_coding_transcript_variant(ENST00000456601)
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)
HES6	hes family bHLH transcription factor 6	2q37.3	Mapped by LD-proxy

SNPs in LD with rs4663865 (count: 0) View in gBrowse (chr2:238237319..238237319 )

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

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