Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.47 (-)
Location

Chromosome 10:98468404 (forward strand) | View in location tab

Co-located

with dbSNP rs4145259 (C/A/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs376062733

This variation has 5 HGVS names - click the plus to show

Variation displays