Original source

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

Alleles
TGCC/- | MAF: 0.32 (-)
Location

Chromosome 7:103524540-103524543 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs150719229, rs146229305

This variant has 5 HGVS names - click the plus to show

About this variant

Variant displays