SNP Report

Basic Info

Name	rs2167571 dbSNP Ensembl
Location	chr2:174734548 - 174734548(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.363818
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000442996); non_coding_transcript_variant(ENST00000442996)
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 rs2167571 (count: 0) View in gBrowse (chr2:174734548..174734548 )

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

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