Original source

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

Alleles
-/G
Location

Chromosome 5: between 148071676 and 148071677 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs66541520

This variation has 10 HGVS names - click the plus to show

Variation displays