SNP Report

Basic Info
Name rs7300145 dbSNP Ensembl
Location chr12:79668376 - 79668376(1)
Variant Alleles T/C
Ancestral Allele C
Minor Allele C
Minor Allele Frequence 0.29972
Functional Annotation intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000328827, ENST00000550006, ENST00000551712); non_coding_transcript_exon_variant(ENST00000547571); non_coding_transcript_variant(ENST00000547571, ENST00000550006)
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)
PAWR PRKC, apoptosis, WT1, regulator 12q21.2 1(0/1/0)

SNPs in LD with rs7300145 (count: 0) View in gBrowse (chr12:79668376..79668376 )

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

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