Original source

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

A/G | Ancestral: A | Ambiguity code: R

Chromosome 1:11018836 (forward strand) | View in location tab


with HGMD-PUBLIC CM081838

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 35 HGVS names - click the plus to show

Variation displays