SNP Report

Basic Info

Name	rs1047631 dbSNP Ensembl
Location	chr6:15522870 - 15522870(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.129193
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000344537, ENST00000355917, ENST00000462989, ENST00000510395, ENST00000513680, ENST00000515875, ENST00000622898, LRG_588t1); downstream_gene_variant(ENST00000338950, ENST00000341776, ENST00000397311, ENST00000506844, ENST00000509674, ENST00000511762, ENST00000514651, LRG_588t2); NMD_transcript_variant(ENST00000510395, ENST00000513680, ENST00000515875); upstream_gene_variant(ENST00000614916)
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)
JARID2	jumonji, AT rich interactive domain 2	6p24-p23	Mapped by Literature SNP
DTNBP1	dystrobrevin binding protein 1	6p22.3	8(4/3/1)

SNPs in LD with rs1047631 (count: 0) View in gBrowse (chr6:15522870..15522870 )

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

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