Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)
Location

Chromosome 6:144066561 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58413870, rs386547876

HGVS name

6:g.144066561G>A

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

About this variant

This variant overlaps 10 transcripts and has 2512 individual genotypes.

Variation displays