Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.13 (G)
Location

Chromosome 10:49607650 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.49607650A>G

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2868 individual genotypes.

Variation displays