Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 4:186196075 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041499

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_207352.3:c.400G>T

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays