Original source

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

Alleles
-/T | MAF: 0.24 (T)
Location

Chromosome 8: between 23050293 and 23050294 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2514 individual genotypes.

Variation displays