Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 5:151851406 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM086829, CM940871, CM940872

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2264, NM_000171.3:c.896G>A, 2265, NM_000171.3:c.896G>T

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and is associated with 3 phenotypes.

Variation displays