SNP Report

Basic Info

Name	rs17727261 dbSNP Ensembl
Location	chr2:124524333 - 124524333(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0179712
Functional Annotation	missense_variant. Polyphen Annotation: benign(ENST00000431078) SIFT Annotation: tolerated(ENST00000431078)
Consequence to Transcript	missense_variant(ENST00000431078)
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)
CNTNAP5	contactin associated protein-like 5	2q14.1	2(0/2/0)

SNPs in LD with rs17727261 (count: 0) View in gBrowse (chr2:124524333..124524333 )

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

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