Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 6:98835062 (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 2 transcripts.

Variant displays