Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.01 (G)
Location

Chromosome 10:48400126 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 7 HGVS names - click the plus to show

About this variant

Variant displays