Original source

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

Alleles
C/-|Ancestral: C|MAF: 0.30 (-)
Location

Chromosome 18:5467381 (forward strand)|View in location tab

Co-located variant

dbSNP rs562214351 (C/A)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 13 HGVS names - Show

About this variant

Variant displays