Original source

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


Chromosome 6: between 10411048 and 10411049 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 19 transcripts and 1 regulatory feature.

Variant displays