Original source

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

-/A | MAF: 0.04 (A)

Chromosome 16: between 79593710 and 79593711 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs374147843

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1092 individual genotypes.

Variation displays