SNP Report

Basic Info

Name	rs11607883 dbSNP Ensembl
Location	chr11:45818158 - 45818158(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.324681
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000534128); non_coding_transcript_variant(ENST00000534128)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs11607883 (count: 0) View in gBrowse (chr11:45818158..45818158 )

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

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