Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 1:17003667 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

This variant has 10 HGVS names - click the plus to show

About this variant

Variant displays