Original source

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

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

Chromosome 17:42787494 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012651

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_032387.4:c.1693C>G, 10654

This variation has 6 HGVS names - click the plus to show

Variation displays