Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:156813852 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 10 HGVS names - click the plus to show

About this variant

Variant displays