Original source

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

G/C/T | Ancestral: G | Ambiguity code: B

Chromosome 1:11022290 (forward strand) | View in location tab


with HGMD-PUBLIC CM091849, CM081449

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 48 HGVS names - click the plus to show

Variation displays