Original source

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

T/G | Ancestral: T | Ambiguity code: K

Chromosome 18:55525291 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 38 HGVS names - click the plus to show

About this variant

This variant overlaps 37 transcripts and has 242 individual genotypes.

Variation displays