Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.02 (A)
Location

Chromosome 6:161350187 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030928

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_019766

This variation has 14 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays