Original source

Variants (including SNPs and indels) imported from dbSNP (release 139)|View in dbSNP

Alleles
C/T|Ambiguity code: Y
Location

Chromosome 10:29368281 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript.

Variant displays