Original source

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

Alleles
-/AATG/ATGA
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 4 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 2 transcripts and has 46 sample genotypes.

Variant displays