Original source

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


Chromosome 8: between 118927569 and 118927570 (forward strand) | View in location tab


with dbSNP rs397706964 (-/T)

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 1 sample genotype.

Variant displays