SNP Report

Basic Info

Name	rs3747066 dbSNP Ensembl
Location	chr22:19850052 - 19850052(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.230232
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000328554, ENST00000405640, ENST00000407472); downstream_gene_variant(ENST00000416337); intron_variant(ENST00000329517, ENST00000403325, ENST00000405009, ENST00000453108, ENST00000460402, ENST00000481086, ENST00000484072); non_coding_transcript_variant(ENST00000460402, ENST00000481086, ENST00000484072)
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)
GNB1L	guanine nucleotide binding protein (G protein), beta polypeptide 1-like	22q11.2	1(1/0/0)
C22orf29	chromosome 22 open reading frame 29	22q11.21	Mapped by LD-proxy

SNPs in LD with rs3747066 (count: 0) View in gBrowse (chr22:19850052..19850052 )

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

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