Original source

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

Alleles
-/T | MAF: 0.03 (T)
Location

Chromosome 12: between 22623508 and 22623509 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2504 individual genotypes.

Variation displays