Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.32 (T)

Chromosome 16:89770464 (forward strand)|View in location tab

Most severe consequence
Splice acceptor variant
Evidence status


Archive dbSNP rs17226624, rs59558950

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts and has 3774 sample genotypes.

Variant displays