Original source

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

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

Chromosome 5:14498585 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Synonyms

Archive dbSNP rs11547880

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 1 sample genotype.

Variant displays