SNP Report

Basic Info

Name	rs5024296 dbSNP Ensembl
Location	chr2:166425242 - 166425242(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.308906
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000409855, ENST00000424326, ENST00000619410, ENST00000621965); NMD_transcript_variant(ENST00000424326)
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)
SCN7A	sodium channel, voltage gated, type VII alpha subunit	2q21-q23	1(0/1/0)

SNPs in LD with rs5024296 (count: 0) View in gBrowse (chr2:166425242..166425242 )

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

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