Original source

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

Alleles
A/G | Ambiguity code: R
Location

Chromosome 17:41239192 (forward strand) | View in location tab

Co-located

with dbSNP rs75748101 (A/G)

Most severe consequence
Evidence status

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

Variation displays