SNP Report

Basic Info

Name	rs7911681 dbSNP Ensembl
Location	chr10:81982939 - 81982939(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.071885
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000372141, ENST00000372142, ENST00000404547, ENST00000404576, ENST00000555784, ENST00000556918, ENST00000602794); NMD_transcript_variant(ENST00000555784, ENST00000602794)
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)
NRG3	neuregulin 3	10q23.1	2(0/2/0)

SNPs in LD with rs7911681 (count: 0) View in gBrowse (chr10:81982939..81982939 )

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

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