Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.43 (A)
Location

Chromosome 1:53128032 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59337212, rs1769311

This variant has 6 HGVS names - click the plus to show

About this variant

Variant displays