This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T | Ancestral: G | Ambiguity code: N | MAF: 0.18 (A)
Location

Chromosome 17:63919146 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts and has 2504 individual genotypes.

Variation displays