Original source

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


Chromosome 10: between 48422048 and 48422049 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs398114297

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 1 sample genotype.

Variant displays