Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 17:80217084 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971353

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_199_SGSH_605270_0003, 13065

This variation has 20 HGVS names - click the plus to show

Variation displays