SNP Report

Basic Info

Name	rs4291228 dbSNP Ensembl
Location	chr8:32236538 - 32236538(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.241613
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000517967, ENST00000518104, ENST00000519301, ENST00000520407, ENST00000523320, ENST00000523534, ENST00000631040); non_coding_transcript_variant(ENST00000517967, ENST00000523320)
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 rs4291228 (count: 0) View in gBrowse (chr8:32236538..32236538 )

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

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