Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 10:98468404 (forward strand) | View in location tab

Co-located

with dbSNP rs112183298 (C/-)

Most severe consequence
 
Intron variant

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts.

Variant displays