Original source

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

Alleles
T/-|Ancestral: T|MAF: 0.23 (T)
Location

Chromosome 7:103594012 (forward strand)|View in location tab

Co-located variant

dbSNP rs200223611 (T/A)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

Variant displays