SNP Report

Basic Info

Name	rs762250 dbSNP Ensembl
Location	chr21:46395124 - 46395124(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.329872
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000359568, ENST00000480896); non_coding_transcript_variant(ENST00000480896)
No. of Studies	1 (Positive: 0; Negative: 1; Trend: 0)
Source	Literature
Overlap with SZ?	NO
Overlap with MDD?	NO

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Anitha, A., 2008	G/C		Genotypic P-value = 0.126, allelic P-value = 0.12 for BD whe...... Genotypic P-value = 0.126, allelic P-value = 0.12 for BD when compared with controls. More...	none of the SNPs analyzed in our study showed a significant ...... none of the SNPs analyzed in our study showed a significant association with bipolar disorder More...	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
PCNT	pericentrin	21q22.3	1(0/1/0)

SNPs in LD with rs762250 (count: 29) View in gBrowse (chr21:46342460..46543738 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²<=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 29)

rs_ID	Functional Annotation	r²[population]
rs2839257	intron_variant; non_coding_transcript_variant; upstream_gene_variant	1.0[CHB]; 1.0[JPT]
rs2839231	intron_variant; non_coding_transcript_variant	0.896[CHB]
rs2839297	intron_variant; upstream_gene_variant	0.896[CHB]; 1.0[JPT]
rs2839285	intron_variant	0.896[CHB]; 1.0[JPT]
rs11089068	downstream_gene_variant; intron_variant	0.896[CHB]; 1.0[JPT]
rs3747010	intron_variant; non_coding_transcript_variant; upstream_gene_variant	0.896[CHB]; 1.0[JPT]
rs4267585	intron_variant; non_coding_transcript_variant; upstream_gene_variant	0.844[CHB]; 1.0[JPT]
rs1123540	upstream_gene_variant	0.896[CHB]; 1.0[JPT]
rs11089069	intron_variant	0.944[CHB]; 1.0[JPT]
rs7279991	intron_variant	0.896[CHB]; 1.0[JPT]
rs2839299	intron_variant; non_coding_transcript_variant	0.896[CHB]; 1.0[JPT]
rs2839268	intron_variant; non_coding_transcript_variant	0.881[CHB]; 0.925[JPT]
rs12626200	intron_variant	0.808[CHB]; 1.0[JPT]
rs2073374	intron_variant; non_coding_transcript_variant; upstream_gene_variant	1.0[CHB]; 1.0[JPT]
rs2839313	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant	0.896[CHB]; 1.0[JPT]
rs1029262	intron_variant; non_coding_transcript_variant	0.896[CHB]; 1.0[JPT]
rs2839270	downstream_gene_variant; intron_variant	0.881[JPT]
rs2839243	intron_variant; non_coding_transcript_variant	1.0[CHB]; 1.0[JPT]
rs2839261	intron_variant; non_coding_transcript_variant	0.947[CHB]; 1.0[JPT]
rs9980536	intron_variant; non_coding_transcript_variant; upstream_gene_variant	0.842[CHB]
rs2330594	intron_variant; non_coding_transcript_variant	1.0[JPT]
rs2073377	intron_variant; non_coding_transcript_variant; upstream_gene_variant	0.947[CHB]; 1.0[JPT]
rs2839275	intron_variant	0.896[CHB]; 1.0[JPT]
rs2032111	intron_variant	0.896[CHB]; 1.0[JPT]
rs2839265	downstream_gene_variant	0.896[CHB]; 1.0[JPT]
rs11909560	downstream_gene_variant	0.896[CHB]; 1.0[JPT]
rs2839317	intron_variant; non_coding_transcript_variant	0.844[CHB]; 1.0[JPT]
rs2070434	intron_variant; non_coding_transcript_variant	0.846[CHB]; 0.937[JPT]
rs2839276	intron_variant	0.896[CHB]; 1.0[JPT]

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

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