Original source

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

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

Chromosome 17:3518587 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, is associated with 4 phenotypes and is mentioned in 1 citation.

Variant displays