Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.35 (C)
Location

Chromosome 2:184913701 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59623514

This variation has 3 HGVS names - click the plus to show

2:g.184913701A>C
ENST00000613975.1:c.1-19902A>C
ENST00000302277.6:c.256-19902A>C

This variation has assays on 8 chips - click the plus to show

Variation displays