Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 1:11023231 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
HGVS names

This variant has 38 HGVS names - Show

About this variant

This variant overlaps 35 transcripts.

Variant displays