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
Location

Chromosome 4:6301696 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM023690

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_094_WFS1_606201_0018, 13639

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

Variation displays