Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 2:112829641 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60381777, rs386589200

HGVS name

2:g.112829641A>G

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 3574 individual genotypes.

Variation displays