Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 2:127428895 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910320

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 17279

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and is associated with 2 phenotypes.

Variation displays