Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 10:100989162 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM074977

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 19669, NM_021830.3:c.952G>A

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 27 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays