Original source

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

Alleles
TC/- | MAF: 0.08 (TC)
Location

Chromosome 11:108119642-108119643 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

About this variant

This variant overlaps 8 transcripts and has 2510 individual genotypes.

Variation displays