Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 1:53213501 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960423

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

Variation displays