Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 1:183574507 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CP973607

Most severe consequence
Clinical significance

Synonyms

LSDB 17279_2

This variation has 11 HGVS names - click the plus to show

Variation displays