Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.34 (A)
Location

Chromosome 2:232542095 (forward strand) | View in location tab

Co-located

with dbSNP rs200832914 (A/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57142893

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

About this variant

This variant overlaps 3 transcripts and has 2507 individual genotypes.

Variation displays