SNP Report

Basic Info

Name	rs7626779 dbSNP Ensembl
Location	chr3:21571542 - 21571542(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.262979
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000281523, ENST00000412369, ENST00000446749, ENST00000478967, ENST00000494108, ENST00000494118); NMD_transcript_variant(ENST00000446749); non_coding_transcript_variant(ENST00000412369, ENST00000478967, ENST00000494108, ENST00000494118)
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)
ZNF385D	zinc finger protein 385D	3p24.3	1(0/1/0)
ZNF385D-AS1	ZNF385D antisense RNA 1	3p24.3	Mapped by Literature SNP

SNPs in LD with rs7626779 (count: 0) View in gBrowse (chr3:21571542..21571542 )

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

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