SNP Report

Basic Info

Name	rs7907743 dbSNP Ensembl
Location	chr10:18364263 - 18364263(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.349641
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000282343, ENST00000324631, ENST00000352115, ENST00000377319, ENST00000377328, ENST00000377329, ENST00000377331, ENST00000396576, ENST00000498816, ENST00000612134, ENST00000612743, ENST00000615785, ENST00000617363); non_coding_transcript_variant(ENST00000498816)
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)
CACNB2	calcium channel, voltage-dependent, beta 2 subunit	10p12	3(2/1/0)

SNPs in LD with rs7907743 (count: 0) View in gBrowse (chr10:18364263..18364263 )

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

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