SNP Report

Basic Info

Name	rs2300237 dbSNP Ensembl
Location	chr12:13660336 - 13660336(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.119808
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000609686, ENST00000636855); non_coding_transcript_variant(ENST00000636855)
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 rs2300237 (count: 0) View in gBrowse (chr12:13660336..13660336 )

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

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