Original source

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

This variant has 17 HGVS names - click the plus to show

About this variant

Variant displays