Original source

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

G/C | Ancestral: G | Ambiguity code: S

Chromosome 15:64156761 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance


This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 94 individual genotypes and is associated with 1 phenotype.

Variation displays