Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.17 (A)
Location

Chromosome 4:154570607 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM080365

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays