SNP Report

Basic Info

Name	rs12448391 dbSNP Ensembl
Location	chr16:6250164 - 6250164(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.142772
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000422070, ENST00000547372, ENST00000547605, ENST00000548749, ENST00000550418, ENST00000553186, ENST00000569895); non_coding_transcript_variant(ENST00000548749, ENST00000569895)
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)
RBFOX1	RNA binding protein, fox-1 homolog (C. elegans) 1	16p13.3	6(2/2/2)

SNPs in LD with rs12448391 (count: 0) View in gBrowse (chr16:6250164..6250164 )

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

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