SNP Report

Basic Info

Name	rs514512 dbSNP Ensembl
Location	chr1:60637528 - 60637528(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.423722
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000439156); non_coding_transcript_variant(ENST00000439156)
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 rs514512 (count: 0) View in gBrowse (chr1:60637528..60637528 )

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

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