Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.27 (G)
Location

Chromosome 5:180522297 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57157203, rs2662274

HGVS names

This variant has 6 HGVS names - Show

About this variant

Variant displays