Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W
Location

Chromosome 10:48424101 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs17404405, rs3181713

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 12 transcripts.

Variant displays