Original source

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

Alleles
-/ATCA | MAF: 0.06 (ATCA)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs148172943

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

Variation displays