SNP Report

Basic Info

Name	rs10233396 dbSNP Ensembl
Location	chrCHR_HSCHR7_2_CTG7:157719598 - 157719598(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.417931
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000389413, ENST00000389416, ENST00000389418, ENST00000409483)
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)
PTPRN2	protein tyrosine phosphatase, receptor type, N polypeptide 2	7q36	1(0/0/1)

SNPs in LD with rs10233396 (count: 0) View in gBrowse (chrCHR_HSCHR7_2_CTG7:157719598..157719598 )

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

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