Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S
Location

Chromosome 10:48424143 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3181715, rs17400430

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 12 transcripts.

Variant displays