Original source

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

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

Chromosome 4:88067937 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM098191

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_058829

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays