Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 10:74082499 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062022

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 27237

This variation has 11 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays