Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 2:73847573 (forward strand) | View in location tab

Most severe consequence

This variation has 13 HGVS names - click the plus to show

Variation displays