SNP Report

Basic Info

Name	rs7864759 dbSNP Ensembl
Location	chr9:114419325 - 114419325(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.247804
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000265134, ENST00000362057, ENST00000374059)
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)
DFNB31	deafness, autosomal recessive 31	9q32	3(2/1/0)

SNPs in LD with rs7864759 (count: 0) View in gBrowse (chr9:114419325..114419325 )

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

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