Original source

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

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

Chromosome 17:39665865 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM025914 ; PhenCode TCAP:c.260G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12689

This variation has 8 HGVS names - click the plus to show

Variation displays