SNP Report

Basic Info

Name	rs268897 dbSNP Ensembl
Location	chr19:50989451 - 50989451(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.423522
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000594512); non_coding_transcript_variant(ENST00000594512)
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 rs268897 (count: 0) View in gBrowse (chr19:50989451..50989451 )

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

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