Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.28 (A)
Location

Chromosome 17:76138591 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Hide

17:g.76138591C>A
ENST00000322957.6:c.499-471G>T

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

Variant displays