Original source

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

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

Chromosome 2:185778428 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59623514

This variation has 2 HGVS names - click the plus to show

2:g.185778428A>C
ENST00000302277.6:c.256-19902A>C

This variation has assays on 7 chips - click the plus to show

Variation displays