Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V
Location

Chromosome 19:10116077 (forward strand)|View in location tab

Most severe consequence
 
Splice region variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 46 transcripts.

Variant displays