Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
-/G | MAF: 0.09 (G)
Location

Chromosome 10: between 112961256 and 112961257 (forward strand) | View in location tab

Most severe consequence

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts and has 1092 individual genotypes.

Variation displays