Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.11 (G)
Location

Chromosome 9:711396 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 2 synonyms - click the plus to show

This variant has 11 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant overlaps 6 transcripts and has 2806 sample genotypes.

Variant displays