Original source

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

Alleles
-/ATTT
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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