Original source

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

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

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

Co-located

with dbSNP rs200223611 (T/A)

Most severe consequence
 
Intron variant
Evidence status

This variant has 4 HGVS names - click the plus to show

About this variant

Variant displays