Original source

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

Alleles
-/A|MAF: 0.30 (A)
Location

Chromosome 4: between 120697801 and 120697802 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2512 sample genotypes.

Variant displays