Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 19:8974691 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_056603

This variation has 3 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 1 transcript and has 264 individual genotypes.

Variation displays