Original source

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

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

Chromosome 10:98490103 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM103400

Most severe consequence
Evidence status

Clinical significance

This variation has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and is associated with 2 phenotypes.

Variation displays