Original source

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

HGVS names

This variant has 5 HGVS names - Show

About this variant

Variant displays