Original source

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

G/A/C | Ancestral: G | Ambiguity code: V

Chromosome 6:10404512 (forward strand) | View in location tab


with HGMD-PUBLIC CM085952

Most severe consequence

This variation has 3 synonyms - click the plus to show

This variation has 42 HGVS names - click the plus to show

About this variant

This variant overlaps 37 transcripts.

Variation displays