SNP Report

Basic Info
Name rs7359083 dbSNP Ensembl
Location chr14:68103744 - 68103744(1)
Variant Alleles A/C
Ancestral Allele A
Minor Allele C
Minor Allele Frequence 0.114417
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000460526, ENST00000468382, ENST00000469165, ENST00000471583, ENST00000478014, ENST00000479335, ENST00000487270, ENST00000487861, ENST00000488612, ENST00000492236, ENST00000497460, ENST00000553595, ENST00000554244, ENST00000557045); NMD_transcript_variant(ENST00000479335); non_coding_transcript_variant(ENST00000460526, ENST00000468382, ENST00000469165, ENST00000478014, ENST00000492236, ENST00000497460, ENST00000553595, ENST00000554244, ENST00000557045)
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)
RAD51B RAD51 paralog B 14q23-q24.2 1(0/1/0)

SNPs in LD with rs7359083 (count: 0) View in gBrowse (chr14:68103744..68103744 )

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

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