Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 15:63060899 (forward strand) | View in location tab


with HGMD-PUBLIC CM941333 ; PhenCode FHC0622 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 42 HGVS names - click the plus to show

About this variant

This variant overlaps 32 transcripts, is associated with 4 phenotypes and is mentioned in 19 citations.

Variation displays