Original source

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

Alleles
G/- | Ancestral: G
Location

Chromosome 17:58996808 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs371731079

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

About this variant

This variant overlaps 6 transcripts and 1 regulatory feature.

Variant displays