SNP Report

Basic Info

Name	rs4236599 dbSNP Ensembl
Location	chr7:114678042 - 114678042(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.208866
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000350908, ENST00000393489, ENST00000393491, ENST00000393494, ENST00000393498, ENST00000403559, ENST00000408937, ENST00000412402, ENST00000634411, ENST00000634664, ENST00000635109, ENST00000635534, ENST00000635638); NMD_transcript_variant(ENST00000412402, ENST00000635109); non_coding_transcript_variant(ENST00000634664)
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)
FOXP2	forkhead box P2	7q31	2(0/2/0)

SNPs in LD with rs4236599 (count: 0) View in gBrowse (chr7:114678042..114678042 )

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

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