SNP Report

Basic Info

Name	rs11022817 dbSNP Ensembl
Location	chr11:13424748 - 13424748(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.392971
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000278174, ENST00000525108, ENST00000525661, ENST00000525864, ENST00000526841, ENST00000527102, ENST00000528120, ENST00000529708, ENST00000530907, ENST00000532261); NMD_transcript_variant(ENST00000525108, ENST00000527102); non_coding_transcript_variant(ENST00000525661, ENST00000525864, ENST00000532261)
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)
BTBD10	BTB (POZ) domain containing 10	11p15.2	Mapped by Literature SNP

SNPs in LD with rs11022817 (count: 0) View in gBrowse (chr11:13424748..13424748 )

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

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