SNP Report

Basic Info

Name	rs3911863 dbSNP Ensembl
Location	chr2:65532630 - 65532630(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.439896
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000377977, ENST00000606978); non_coding_transcript_variant(ENST00000377977, ENST00000606978)
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 rs3911863 (count: 0) View in gBrowse (chr2:65532630..65532630 )

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

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