Original source

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


Chromosome 7: between 101129661 and 101129662 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs140253428

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and has 4 sample genotypes.

Variant displays