SNP Report

Basic Info

Name	rs2808078 dbSNP Ensembl
Location	chr10:31883624 - 31883624(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.486621
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000311380, ENST00000344936, ENST00000375245, ENST00000375250, ENST00000396144)
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)
ARHGAP12	Rho GTPase activating protein 12	10p11.22	Mapped by LD-proxy

SNPs in LD with rs2808078 (count: 0) View in gBrowse (chr10:31883624..31883624 )

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

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