Original source

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

Alleles
T/-
Location

Chromosome 15:40724890 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs71104731, rs71428305

This variation has 8 HGVS names - click the plus to show

Variation displays