SNP Report

Basic Info

Name	rs11178971 dbSNP Ensembl
Location	chr12:71867975 - 71867975(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.122604
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000319106, ENST00000462788, ENST00000468049, ENST00000472611, ENST00000474468, ENST00000482439, ENST00000485960, ENST00000491063, ENST00000498482, ENST00000546932, ENST00000549402, ENST00000550746); NMD_transcript_variant(ENST00000462788, ENST00000468049, ENST00000472611, ENST00000498482); non_coding_transcript_variant(ENST00000474468, ENST00000546932, ENST00000549402); upstream_gene_variant(ENST00000460818)
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)
TBC1D15	TBC1 domain family, member 15	12q15	Mapped by Literature SNP

SNPs in LD with rs11178971 (count: 0) View in gBrowse (chr12:71867975..71867975 )

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

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