Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V | MAF: < 0.01 (G)
Location

Chromosome 3:93879306 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961186, CM951058

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays