Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 17:7283555 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_012060

This variation has 12 HGVS names - click the plus to show

Variation displays