This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/G/T/C | Ancestral: A | Ambiguity code: N

Chromosome 17:43115745 (forward strand) | View in location tab


with HGMD-PUBLIC CM087249, CM041683, CM040687

Most severe consequence
Clinical significance


LSDB U14680.1:c.115T>C, U14680.1:c.115T>A

This variation has 120 HGVS names - click the plus to show

About this variant

This variant overlaps 66 transcripts and is associated with 5 phenotypes.

Variation displays