Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.02 (G)
Location

Chromosome 10:6142899 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60417247

HGVS name

10:g.6142899G>A

About this variant

This variant overlaps 2 transcripts and has 2512 individual genotypes.

Variation displays