Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.30 (C)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386528769, 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 9 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 4230 individual genotypes, is associated with 1 phenotype and is mentioned in 87 citations.

Variation displays