Original source

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

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

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

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs3811783, rs61392673

This variant has 9 HGVS names - click the plus to show

About this variant

Variant displays