Original source

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

Alleles
T/-/G | Ancestral: T
Location

Chromosome 5:68241387 (forward strand) | View in location tab

Co-located

with dbSNP rs2545410 (T/G)

Most severe consequence
Evidence status

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

Variation displays