SNP Report

Basic Info

Name	rs9648369 dbSNP Ensembl
Location	chr7:30569046 - 30569046(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.404952
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000426529, ENST00000578245, ENST00000579024, ENST00000581665, ENST00000581794, ENST00000582145, ENST00000582733, ENST00000584108, ENST00000584199, ENST00000584372, ENST00000584621, ENST00000614950); non_coding_transcript_variant(ENST00000426529, ENST00000578245, ENST00000579024, ENST00000581665, ENST00000581794, ENST00000582145, ENST00000582733, ENST00000584108, ENST00000584199, ENST00000584372, ENST00000584621, ENST00000614950); upstream_gene_variant(ENST00000355837, ENST00000621272)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs9648369 (count: 0) View in gBrowse (chr7:30569046..30569046 )

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

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