SNP Report

Basic Info

Name	rs12150048 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45761700 - 45761700(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.0952476
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000587305, ENST00000634540); non_coding_transcript_variant(ENST00000587305, ENST00000631500, ENST00000632599, ENST00000631500, ENST00000632599)
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 rs12150048 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45761700..45761700 )

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

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