SNP Report

Basic Info

Name	rs4531002 dbSNP Ensembl
Location	chr8:32644468 - 32644468(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.234225
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000287842, ENST00000356819, ENST00000405005, ENST00000518104, ENST00000518206, ENST00000519301, ENST00000520407, ENST00000521670, ENST00000522569, ENST00000523079, ENST00000523534, ENST00000631040); non_coding_transcript_variant(ENST00000522569); upstream_gene_variant(ENST00000520502, ENST00000523041)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
NRG1	neuregulin 1	8p12	15(10/5/0)

SNPs in LD with rs4531002 (count: 0) View in gBrowse (chr8:32644468..32644468 )

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

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