Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.05 (A)
Location

Chromosome 9:37430655 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_012203.1:c.734+9G>A

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 13 transcripts, has 2506 sample genotypes and is associated with 1 phenotype.

Variant displays