Original source

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

Alleles
AAAC/-|MAF: 0.37 (AAAC)
Location

Chromosome 11:18405840-18405843 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs148072862, rs143718787

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 23 transcripts and has 2513 sample genotypes.

Variant displays