Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B
Location

Chromosome 17:43115750 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041681, CM101974

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB U14680.1:c.110C>G, U14680.1:c.110C>A

This variation has 80 HGVS names - click the plus to show

About this variant

This variant overlaps 44 transcripts and is associated with 4 phenotypes.

Variation displays