Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 3 HGVS names - click the plus to show

About this variant

Variant displays