Original source

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

Alleles
-/G|MAF: 0.48 (-)
Location

Chromosome 11: between 102598048 and 102598049 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs149118200, rs56736408

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays