SNP Report

Basic Info

Name	rs36007753 dbSNP Ensembl
Location	chr21:44375991 - 44375991(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele Frequence	0.0
Functional Annotation	non_coding_transcript_exon_variant; non_coding_transcript_variant; synonymous_variant.
Consequence to Transcript	non_coding_transcript_exon_variant(ENST00000498430); non_coding_transcript_variant(ENST00000498430); synonymous_variant(ENST00000300481, ENST00000300482, ENST00000397928, ENST00000397932)
No. of Studies	1 (Positive: 0; Negative: 0; Trend: 1)
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
McQuillin, A., 2006			no P-value no P-value	novel Polymorphisms identified in this study novel Polymorphisms identified in this study	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
TRPM2	transient receptor potential cation channel, subfamily M, member 2	21q22.3	5(3/2/0)

SNPs in LD with rs36007753 (count: 0) View in gBrowse (chr21:44375991..44375991 )

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

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