SNP Report

Basic Info

Name	rs546966 dbSNP Ensembl
Location	chr18:10535916 - 10535916(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.338059
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000580746); intron_variant(ENST00000322897, ENST00000580224, ENST00000580483, ENST00000582472, ENST00000582978); NMD_transcript_variant(ENST00000580224, ENST00000580483); non_coding_transcript_variant(ENST00000582978); upstream_gene_variant(ENST00000583367)
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)
NAPG	N-ethylmaleimide-sensitive factor attachment protein, gamma	18p11.21	3(2/1/0)

SNPs in LD with rs546966 (count: 0) View in gBrowse (chr18:10535916..10535916 )

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

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