SNP Report

Basic Info

Name	rs2301622 dbSNP Ensembl
Location	chr12:111457399 - 111457399(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.464657
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000377617, ENST00000389153, ENST00000389154, ENST00000482777, ENST00000483311, ENST00000535949, ENST00000542287, ENST00000550104, ENST00000550844, ENST00000550889, ENST00000608853, ENST00000616825); NMD_transcript_variant(ENST00000483311); non_coding_transcript_exon_variant(ENST00000468920, ENST00000551551); non_coding_transcript_variant(ENST00000468920, ENST00000482777, ENST00000550889, ENST00000551551); upstream_gene_variant(ENST00000475132, ENST00000484991)
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)
ATXN2	ataxin 2	12q23-q24.1	Mapped by LD-proxy

SNPs in LD with rs2301622 (count: 0) View in gBrowse (chr12:111457399..111457399 )

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

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