Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.11 (T)
Location

Chromosome 16:108663 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57802088, rs798611

This variation has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2505 individual genotypes.

Variation displays