Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.33 (C)
Location

Chromosome 4:53378154 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs3811783, rs61392673

HGVS names

This variant has 9 HGVS names - Show

About this variant

Variant displays