Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.27 (C)

Chromosome 19:21114091 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs4318333

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2509 sample genotypes.

Variant displays