Original source

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

Alleles
-/A | MAF: 0.26 (A)
Location

Chromosome 10: between 99535896 and 99535897 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

About this variant

This variant overlaps 3 transcripts and has 2506 individual genotypes.

Variation displays