Original source

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

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

Chromosome 15:48490038 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 279 individual genotypes and is associated with 2 phenotypes.

Variation displays