Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

HGMD-PUBLIC CM920720

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 16951, 2010_April_001_076_XPA_611153_0005

HGVS names

This variant has 9 HGVS names - Show

About this variant

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

Variant displays