Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.39 (A)
Location

Chromosome 10:124986120 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3168030

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

About this variant

This variant overlaps 8 transcripts and has 2536 individual genotypes.

Variation displays