Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 2:219420939 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980537 ; PhenCode HIFD_DES:c.1009G>C (G/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

Variation displays