Original source

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

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

Chromosome 14:20475175 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961049 ; PhenCode NPbase_D0064:g.6766A>G (A/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_038_NP_164050_0006, 4322

This variation has 9 HGVS names - click the plus to show

Variation displays