Original source

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

Alleles
-/T
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs371079323, rs200559289

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 4 sample genotypes.

Variant displays