Original source

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

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

Chromosome 19:55154047 (forward strand) | View in location tab


with HGMD-PUBLIC CM030287 ; PhenCode FHC0394 (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 29 transcripts and is associated with 2 phenotypes.

Variation displays