SNP Report

Basic Info

Name	rs4764863 dbSNP Ensembl
Location	chr12:102120406 - 102120406(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.431909
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000327680, ENST00000392909, ENST00000392911, ENST00000537257, ENST00000541394, ENST00000543784); NMD_transcript_variant(ENST00000392909); non_coding_transcript_exon_variant(ENST00000541668); non_coding_transcript_variant(ENST00000541668); upstream_gene_variant(ENST00000251074, ENST00000392914, ENST00000412715, ENST00000417507, ENST00000457614, ENST00000535811, ENST00000543021, ENST00000548994, ENST00000550459, ENST00000551200, ENST00000551744, ENST00000552283)
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)
NUP37	nucleoporin 37kDa	12q23.2	Mapped by LD-proxy
PARPBP	PARP1 binding protein	12q23.2	Mapped by LD-proxy

SNPs in LD with rs4764863 (count: 0) View in gBrowse (chr12:102120406..102120406 )

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

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