Original source

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

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

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

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

About this variant

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

Variation displays