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

Co-located

with dbSNP rs5886002 (A/C/G/T)

Most severe consequence
Evidence status

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

Variation displays