Original source

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

Alleles
GGGGGCC/-
Location

Chromosome 2:74887436-74887442 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs34415979

This variant has 3 HGVS names - click the plus to show

About this variant

Variant displays