Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.47 (G)
Location

Chromosome 17:44745979 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59134100

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2508 sample genotypes.

Variant displays