SNP Report

Basic Info

Name	rs2952151 dbSNP Ensembl
Location	chr17:39672243 - 39672243(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.428714
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. Polyphen Annotation: unknown(ENST00000619169)
Consequence to Transcript	3_prime_UTR_variant(ENST00000300658, ENST00000378011, ENST00000579146); downstream_gene_variant(ENST00000269582, ENST00000394246, ENST00000429199, ENST00000577337, ENST00000580898, ENST00000581428, ENST00000582276, ENST00000584620); missense_variant(ENST00000619169); non_coding_transcript_exon_variant(ENST00000309862); non_coding_transcript_variant(ENST00000309862)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
PNMT	phenylethanolamine N-methyltransferase	17q12	Mapped by LD-proxy
PGAP3	post-GPI attachment to proteins 3	17q21.2	Mapped by LD-proxy

SNPs in LD with rs2952151 (count: 0) View in gBrowse (chr17:39672243..39672243 )

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

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