Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.39 (-)
Location

Chromosome 11:113452648 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs71063506, rs376927423

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

About this variant

This variant overlaps 6 transcripts and has 2506 individual genotypes.

Variation displays