SNP Report

Basic Info

Name	rs211146 dbSNP Ensembl
Location	chr11:17959500 - 17959500(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.311502
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; synonymous_variant.
Consequence to Transcript	intron_variant(ENST00000525920, ENST00000527494, ENST00000528200, ENST00000529440, ENST00000532265, ENST00000532546); NMD_transcript_variant(ENST00000525422, ENST00000527494, ENST00000532546); non_coding_transcript_exon_variant(ENST00000525168); non_coding_transcript_variant(ENST00000525168, ENST00000529440); synonymous_variant(ENST00000265965, ENST00000525422, ENST00000529151, ENST00000529728, ENST00000533241)
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)
SERGEF	secretion regulating guanine nucleotide exchange factor	11p14.3	Mapped by LD-proxy

SNPs in LD with rs211146 (count: 0) View in gBrowse (chr11:17959500..17959500 )

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

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