Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2507 sample genotypes.

Variant displays