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 | MAF: < 0.01 (C)
Location

Chromosome 17:43115791 (forward strand) | View in location tab

Co-located

with dbSNP rs273902790 (G/-)

Most severe consequence
Evidence status

Synonyms

LSDB U14680.1:c.81-12C>G

This variation has 24 HGVS names - click the plus to show

Variation displays