Original source

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

GTT/- | MAF: 0.09 (-)

Chromosome 15:40722530-40722532 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs374610247

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 1092 individual genotypes.

Variation displays