Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (T)
Location

Chromosome 5:14186124 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57735394, rs1302355

This variant has 6 HGVS names - click the plus to show

About this variant

Variant displays