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 2:27309945 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061855

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2177, NM_002437.4:c.498C>A

This variation has 20 HGVS names - click the plus to show

Variation displays