BDgene

SNP Report

Basic Info
Name rs10982212 dbSNP Ensembl
Location chr9:114425696 - 114425696(1)
Variant Alleles C/G
Ancestral Allele G
Minor Allele G
Minor Allele Frequence 0.347644
Functional Annotation 5_prime_UTR_variant; intron_variant.
Consequence to Transcript 5_prime_UTR_variant(ENST00000374059); intron_variant(ENST00000265134, ENST00000362057)
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)
DFNB31 deafness, autosomal recessive 31 9q32 3(2/1/0)

SNPs in LD with rs10982212 (count: 0) View in gBrowse (chr9:114425696..114425696 )

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

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