Original source

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


Chromosome 17: between 58991193 and 58991194 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs140994674, rs398031215

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays