BDgene

SNP Report

Basic Info
Name rs1320966 dbSNP Ensembl
Location chr1:169145900 - 169145900(1)
Variant Alleles G/C
Ancestral Allele G
Minor Allele C
Minor Allele Frequence 0.251997
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000367811, ENST00000472647, ENST00000493481, ENST00000525440, ENST00000530739); NMD_transcript_variant(ENST00000525440); non_coding_transcript_variant(ENST00000493481, ENST00000530739)
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)
NME7 NME/NM23 family member 7 1q24.2 1(0/1/0)

SNPs in LD with rs1320966 (count: 0) View in gBrowse (chr1:169145900..169145900 )

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

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