Original source

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

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

Chromosome 1:183559335 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM086691, CM101795

Most severe consequence
Evidence status

Clinical significance

Synonyms

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

Variation displays