Original source

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

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 2:208989018 (forward strand) | View in location tab


with HGMD-PUBLIC CM020930, CM072969 ; dbSNP rs76022179 (G/T)

Most severe consequence
Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Variation displays