Original source

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


Chromosome 19: between 49063013 and 49063014 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs140835190, rs71179078

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2 sample genotypes.

Variant displays