SNP Report

Basic Info

Name	rs6679393 dbSNP Ensembl
Location	chr1:31298097 - 31298097(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.410743
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000344147, ENST00000373714, ENST00000479629, ENST00000546109, ENST00000615916, ENST00000616393, ENST00000616859, ENST00000618216, ENST00000627541); non_coding_transcript_variant(ENST00000479629); upstream_gene_variant(ENST00000263694, ENST00000463988)
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)
ZCCHC17	zinc finger, CCHC domain containing 17	1p35.2	Mapped by Literature SNP
SNRNP40	small nuclear ribonucleoprotein 40kDa (U5)	1p35.2	Mapped by LD-proxy

SNPs in LD with rs6679393 (count: 0) View in gBrowse (chr1:31298097..31298097 )

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

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