Original source

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

Alleles
T/C/G | Ancestral: C | Ambiguity code: B | MAF: 0.32 (T)
Location

Chromosome 17:64321170 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386421216, rs117480038

This variation has 4 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 3683 individual genotypes.

Variation displays