SNP Report

Basic Info

Name	rs2276095 dbSNP Ensembl
Location	chr18:9132373 - 9132373(1)
Variant Alleles	A/C
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.221246
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000608008); intron_variant(ENST00000318388, ENST00000400033, ENST00000465096, ENST00000474740, ENST00000578850, ENST00000579126); non_coding_transcript_exon_variant(ENST00000582375, ENST00000583081); non_coding_transcript_variant(ENST00000465096, ENST00000474740, ENST00000578850, ENST00000579126, ENST00000582375, ENST00000583081); upstream_gene_variant(ENST00000262126, ENST00000540578, ENST00000577992, ENST00000581635, ENST00000585234)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ANKRD12	ankyrin repeat domain 12	18p11.22	Mapped by Literature SNP
NDUFV2	NADH dehydrogenase (ubiquinone) flavoprotein 2, 24kDa	18p11.22	6(5/1/0)

SNPs in LD with rs2276095 (count: 0) View in gBrowse (chr18:9132373..9132373 )

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

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