Original source

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

Alleles
C/-|Ancestral: C|MAF: 0.18 (-)
Location

Chromosome 10:112951111 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs368488751, rs147297579

HGVS names

This variant has 17 HGVS names - Show

About this variant

Variant displays