Original source

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

G/- | Ancestral: G

Chromosome 10:62401487 (forward strand) | View in location tab


with dbSNP rs202164670 (G/T)

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 4 transcripts and has 10 individual genotypes.

Variation displays