Original source

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

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

Chromosome 2:9601852 (forward strand) | View in location tab

Most severe consequence

This variation has 5 HGVS names - click the plus to show

Variation displays