SNP Report

Basic Info
Name rs7981120 dbSNP Ensembl
Location chr13:102694309 - 102694309(1)
Variant Alleles G/A
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.474042
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000267273)
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)
METTL21C methyltransferase like 21C 13q33.1 1(1/0/0)

SNPs in LD with rs7981120 (count: 0) View in gBrowse (chr13:102694309..102694309 )

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

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