SNP Report

Basic Info

Name	rs702895 dbSNP Ensembl
Location	chr2:65534933 - 65534933(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.354832
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 rs702895 (count: 0) View in gBrowse (chr2:65534933..65534933 )

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

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