Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:183586922 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM992935

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.

Variation displays