SNP Report

Basic Info
Name rs1991148 dbSNP Ensembl
Location chr2:107396697 - 107396697(1)
Variant Alleles T/A
Ancestral Allele T
Minor Allele T
Minor Allele Frequence 0.439696
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000413708, ENST00000414300, ENST00000422203, ENST00000443833); non_coding_transcript_variant(ENST00000413708, ENST00000414300, ENST00000422203, ENST00000443833)
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 rs1991148 (count: 0) View in gBrowse (chr2:107396697..107396697 )

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

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