Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 10:100989165 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM050079

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_021830.3:c.955A>G, 13534, 2010_April_001_070_PEO1_606075_0010

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 54 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays