Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 12:13564526 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000012.11:g.13717460C>T

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and is associated with 1 phenotype.

Variation displays