Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 4:6302281 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013445

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13636, 2010_April_001_091_WFS1_606201_0015

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

Variation displays