Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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 4593, 2010_April_001_084_PRF1_170280_0008

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

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variation displays