Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 10:70599173 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM992950 ; PhenCode PRF1base_D0067:g.5003T>G (A/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_084_PRF1_170280_0008, 4593

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

Variation displays