Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
-/T
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs371079323, rs200559289

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

Variation displays