Original source

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

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

Chromosome 1:183590200 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM101795, CM086691

Most severe consequence
Evidence status

Clinical significance

Synonyms

This variation has 26 HGVS names - click the plus to show

Variation displays