Original source

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

Alleles
G/-
Location

Chromosome 8:23041061 (forward strand) | View in location tab

Co-located

with dbSNP rs199870003 (G/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs150035574

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

Variation displays