Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386528769, rs59623514

HGVS names

This variant has 3 HGVS names - Hide

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

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 2 transcripts, has 4230 sample genotypes, is associated with 1 phenotype and is mentioned in 101 citations.

Variant displays