Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 9:37436758 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

LSDB NM_012203.1:c.963G>A

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 11 transcripts and has 2504 sample genotypes.

Variant displays