Original source

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


Chromosome 19: between 48978553 and 48978554 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs398121053

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature and has 3 sample genotypes.

Variant displays