Original source

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


Chromosome 7: between 128241953 and 128241954 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 1 transcript and has 46 sample genotypes.

Variant displays