Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 10:48424113 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3181714, rs17400409

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2 sample genotypes.

Variant displays