Original source

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

Alleles
-/G
Location

Chromosome 7: between 97020572 and 97020573 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Variation displays