Original source

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


Chromosome 5: between 132299622 and 132299623 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs397959473

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and has 6 sample genotypes.

Variant displays