BDgene

SNP Report

Basic Info
Name rs166468 dbSNP Ensembl
Location chr2:107418201 - 107418201(1)
Variant Alleles C/T
Ancestral Allele C
Minor Allele C
Minor Allele Frequence 0.418331
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000414300); non_coding_transcript_variant(ENST00000414300)
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 rs166468 (count: 0) View in gBrowse (chr2:107418201..107418201 )

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

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