Original source

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

T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.22 (C)

Chromosome 9:35074920 (forward strand)|View in location tab

Most severe consequence
Splice region variant
Evidence status


Archive dbSNP rs17882272

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 14 transcripts, has 4016 sample genotypes and is mentioned in 1 citation.

Variant displays