Original source

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

Alleles
-/T
Location

Chromosome 10: between 48428993 and 48428994 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs371079323, rs200559289

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 4 sample genotypes.

Variant displays