SNP Report

Basic Info

Name	rs1805544 dbSNP Ensembl
Location	chr12:13634900 - 13634900(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.108227
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 rs1805544 (count: 0) View in gBrowse (chr12:13634900..13634900 )

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

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