Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.41 (G)
Location

Chromosome 10:98456912 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.98456912G>A

About this variant

This variant overlaps 6 transcripts and has 2511 individual genotypes.

Variation displays