Original source

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

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

Chromosome 2:71598661 (forward strand) | View in location tab

Co-located

with PhenCode DYSF:c.3618C>G (C/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000002.10:g.71679299C>T

This variation has 15 HGVS names - click the plus to show

Variation displays