Original source

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

TATT/- | MAF: 0.32 (-)

Chromosome 5:135030019-135030022 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs33953498, rs147022439

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

About this variant

This variant overlaps 10 transcripts and has 1100 individual genotypes.

Variation displays