Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (T)
Location

Chromosome 11:102601215 (forward strand) | View in location tab

Co-located

with dbSNP rs74555342 (C/T)

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

Variation displays