Original source

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

-/ATCA | MAF: 0.06 (ATCA)

Chromosome 5: between 96775339 and 96775340 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs148172943

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 24 transcripts and has 1092 individual genotypes.

Variation displays