Original source

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

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

Chromosome 13:51958333 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960124, CM950111, CP995079

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

About this variant

This variant overlaps 7 transcripts and is associated with 3 phenotypes.

Variation displays