Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D
Location

Chromosome 7:128252162 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS982252

Most severe consequence
 
Splice region variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant overlaps 2 transcripts.

Variant displays