SNP Report

Basic Info

Name	rs2113545 dbSNP Ensembl
Location	chr7:136977994 - 136977994(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.499401
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000320658, ENST00000401861, ENST00000425981, ENST00000439694, ENST00000445907, ENST00000453373, ENST00000586239, ENST00000592183, ENST00000593789, ENST00000597642, ENST00000598184, LRG_405t1, LRG_405t2); non_coding_transcript_variant(ENST00000425981, ENST00000439694, ENST00000586239, ENST00000592183, ENST00000593789, ENST00000597642, ENST00000598184)
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)
CHRM2	cholinergic receptor, muscarinic 2	7q35-q36	1(0/1/0)

SNPs in LD with rs2113545 (count: 0) View in gBrowse (chr7:136977994..136977994 )

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

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