Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 17:43124095 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041678, CM014520

Most severe consequence
Clinical significance

Synonyms

LSDB U14680.1:c.2T>G, U14680.1:c.2T>C

This variation has 84 HGVS names - click the plus to show

Variation displays