Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 9:97684977 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920720

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 16951, 2010_April_001_076_XPA_611153_0005

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

About this variant

This variant overlaps 4 transcripts and is associated with 2 phenotypes.

Variant displays