Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.47 (T)

Chromosome 16:88643329 (forward strand) | View in location tab


with HGMD-PUBLIC CR995275

Most severe consequence
Evidence status


Archive dbSNP rs17701020, rs3189363

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

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 13 transcripts, has 2359 individual genotypes and is mentioned in 6 citations.

Variation displays