Original source

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

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

Chromosome 10:74074820 (forward strand) | View in location tab

Most severe consequence
Synonyms

Uniprot VAR_037667

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

Variation displays