Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
TGCC/- | MAF: 0.39 (-)
Location

Chromosome 7:103164987-103164990 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs150719229, rs146229305

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

Variation displays