SNP Report

Basic Info

Name	rs12897429 dbSNP Ensembl
Location	chr14:57665239 - 57665239(1)
Variant Alleles	C/G/T
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.15635
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000556568, ENST00000556826, ENST00000557430); non_coding_transcript_variant(ENST00000556568, ENST00000557430)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
SLC35F4	solute carrier family 35, member F4	14q22.3	Mapped by Literature SNP

SNPs in LD with rs12897429 (count: 0) View in gBrowse (chr14:57665239..57665239 )

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

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