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)