Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/ATTT
Location

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

Most severe consequence
Synonyms

Archive dbSNP rs398114297

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 1 individual genotype.

Variation displays