SNP Report

Basic Info

Name	rs6976 dbSNP Ensembl
Location	chr3:52694788 - 52694788(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.304712
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000266014, ENST00000394783, ENST00000478968, ENST00000481643, ENST00000491606); downstream_gene_variant(ENST00000391150, ENST00000394799, ENST00000410413, ENST00000418458, ENST00000459623, ENST00000463827, ENST00000479553, ENST00000480080, ENST00000484022, ENST00000484163, ENST00000485899, ENST00000487642, ENST00000489119, ENST00000492349, ENST00000496254, ENST00000497356, ENST00000497436, ENST00000497953); NMD_transcript_variant(ENST00000481643)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 4)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
GLT8D1	glycosyltransferase 8 domain containing 1	3p21.1	1(1/0/0)
SNORD69	small nucleolar RNA, C/D box 69	3p21.1	Mapped by Literature SNP
GNL3	guanine nucleotide binding protein-like 3 (nucleolar)	3p21.1	2(2/0/0)
SNORD19B	small nucleolar RNA, C/D box 19B	3p21.1	Mapped by Literature SNP

SNPs in LD with rs6976 (count: 0) View in gBrowse (chr3:52694788..52694788 )

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

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