Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 19:48969810 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_014731

This variant has 5 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 10 transcripts and has 267 sample genotypes.

Variant displays