Original source

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

Alleles
-/T
Location

Chromosome 5: between 148082983 and 148082984 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs375112446, rs200103553

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

Variation displays