Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP


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

Most severe consequence
Evidence status


Archive dbSNP rs397959473

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 6 individual genotypes.

Variation displays