Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

TGCC/- | MAF: 0.39 (-)

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

Most severe consequence
Evidence status


Archive dbSNP rs150719229, rs146229305

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

About this variant

This variant overlaps 5 transcripts and has 1096 individual genotypes.

Variation displays