Original source

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


Chromosome 8: between 127413880 and 127413881 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs386360972

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and has 8 sample genotypes.

Variant displays