Original source

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

Alleles
TA/-|MAF: 0.28 (-)
Location

Chromosome 10:52769916-52769917 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs141956473

HGVS names

This variant has 4 HGVS names - Show

About this variant

Variant displays