SNP Report

Basic Info

Name	rs11158721 dbSNP Ensembl
Location	chr14:68129118 - 68129118(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.136382
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, ENST00000554679, ENST00000557045); NMD_transcript_variant(ENST00000479335); non_coding_transcript_variant(ENST00000460526, ENST00000468382, ENST00000469165, ENST00000478014, ENST00000492236, ENST00000497460, ENST00000553595, ENST00000554244, ENST00000554679, 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 rs11158721 (count: 0) View in gBrowse (chr14:68129118..68129118 )

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

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