SNP Report

Basic Info

Name	rs8053440 dbSNP Ensembl
Location	chr16:8804601 - 8804601(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.185104
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000566196); intron_variant(ENST00000268261, ENST00000562318, ENST00000562448, ENST00000564030, ENST00000564069, ENST00000565221, ENST00000565896, ENST00000566540, ENST00000566604, ENST00000566983, ENST00000568602, ENST00000569958, ENST00000570076, ENST00000570134); NMD_transcript_variant(ENST00000562318, ENST00000564069, ENST00000565221, ENST00000565896, ENST00000566540, ENST00000566604, ENST00000568602, ENST00000570076, ENST00000570134); non_coding_transcript_variant(ENST00000562448, ENST00000564030); upstream_gene_variant(ENST00000567697)
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)
PMM2	phosphomannomutase 2	16p13	Mapped by LD-proxy

SNPs in LD with rs8053440 (count: 0) View in gBrowse (chr16:8804601..8804601 )

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

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