Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.44 (C)
Location

Chromosome 17:34358987 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs56522587, rs59584284

HGVS name

17:g.34358987T>C

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 3 transcripts and has 3580 sample genotypes.

Variant displays