Original source

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

Alleles
AT/-|MAF: 0.06 (-)
Location

Chromosome 17:58993799-58993800 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs372114650, rs149614969

HGVS names

This variant has 4 HGVS names - Show

About this variant

Variant displays