Original source

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

Alleles
-/C | MAF: 0.48 (-)
Location

Chromosome 10: between 112967049 and 112967050 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs144667283

This variant has 16 HGVS names - click the plus to show

About this variant

Variant displays