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 1:153259362 (forward strand) | View in location tab

Co-located

with dbSNP rs370880484 (C/-/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs111764845

HGVS name

1:g.153259362C>G

Variation displays