SNP Report

Basic Info

Name	rs6787318 dbSNP Ensembl
Location	chr3:197742767 - 197742767(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.261382
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000273582, ENST00000428738, ENST00000467303); non_coding_transcript_variant(ENST00000467303)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
FYTTD1	forty-two-three domain containing 1	3q29	1(0/1/0)
KIAA0226	KIAA0226	3q29	Mapped by Literature SNP

SNPs in LD with rs6787318 (count: 0) View in gBrowse (chr3:197742767..197742767 )

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

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