SNP Report

Basic Info

Name	rs12368121 dbSNP Ensembl
Location	chr12:103857394 - 103857394(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.170128
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000548527, ENST00000551270); non_coding_transcript_variant(ENST00000548527, ENST00000551270)
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 rs12368121 (count: 0) View in gBrowse (chr12:103857394..103857394 )

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

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