Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.04 (C)
Location

Chromosome 7:44164135 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 4 HGVS names - click the plus to show

About this variant

Variant displays