SNP Report

Basic Info

Name	rs11080114 dbSNP Ensembl
Location	chr17:30080269 - 30080269(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.429313
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000394835, ENST00000419434, ENST00000588978)
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)
EFCAB5	EF-hand calcium binding domain 5	17q11.2	Mapped by Literature SNP

SNPs in LD with rs11080114 (count: 0) View in gBrowse (chr17:30080269..30080269 )

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

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