Original source

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

Alleles
-/A | MAF: < 0.01 (-)
Location

Chromosome 7: between 128244086 and 128244087 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2507 sample genotypes.

Variant displays