SNP Report

Basic Info

Name	rs2069612 dbSNP Ensembl
Location	chr14:96250346 - 96250346(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.146565
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000553811, ENST00000555847); non_coding_transcript_variant(ENST00000555847)
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 rs2069612 (count: 0) View in gBrowse (chr14:96250346..96250346 )

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

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