Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Clinical significance

Synonyms

LSDB 16951, 2010_April_001_076_XPA_611153_0005

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

Variation displays