Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

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

Variation displays