Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 2:9601852 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts.

Variant displays