Original source

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

Alleles
G/-|Ancestral: G|MAF: 0.28 (-)
Location

Chromosome 2:174751339 (forward strand)|View in location tab

Co-located variant

dbSNP rs149000086 (G/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs144230187, rs371511301

HGVS names

This variant has 7 HGVS names - Show

About this variant

Variant displays