Original source

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

Alleles
T/-/C | Ancestral: C
Location

Chromosome 19:10285806 (forward strand) | View in location tab

Co-located

with dbSNP rs10420338 (T/C)

Most severe consequence
Evidence status

This variation has 18 HGVS names - click the plus to show

Variation displays