SNP Report

Basic Info
Name rs1119377 dbSNP Ensembl
Location chr8:101974574 - 101974574(1)
Variant Alleles G/T
Ancestral Allele T
Minor Allele T
Minor Allele Frequence 0.380391
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000311028, ENST00000395923, ENST00000517531, ENST00000517639, ENST00000517822, ENST00000518166, ENST00000518661, ENST00000518727, ENST00000518952, ENST00000520425, ENST00000520690, ENST00000521599, ENST00000521964, ENST00000522078, ENST00000522206, ENST00000523923, ENST00000524209); non_coding_transcript_variant(ENST00000517639, ENST00000518952)
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)
NCALD neurocalcin delta 8q22.3 1(0/1/0)

SNPs in LD with rs1119377 (count: 0) View in gBrowse (chr8:101974574..101974574 )

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

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