Original source

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

-/G | MAF: 0.23 (-)

Chromosome 19: between 16485848 and 16485849 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs376552064

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 1098 individual genotypes.

Variation displays