Original source

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

Alleles
C/- | Ancestral: C
Location

Chromosome 17:4901885 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs377046464, rs144972793

This variation has 4 HGVS names - click the plus to show

Variation displays