Original source

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

Alleles
-/T
Location

Chromosome 4: between 119134547 and 119134548 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs146386132

This variation has 2 HGVS names - click the plus to show

Variation displays