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 2:127423087 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CX067274

Most severe consequence
Synonyms

LSDB PC-HY12

This variation has 14 HGVS names - click the plus to show

Variation displays