Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 5:253094 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_Human610_Quad

About this variant

This variant overlaps 14 transcripts and has 514 sample genotypes.

Variant displays