Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/-|Ancestral: T
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 10 HGVS names - Show

About this variant

Variant displays