Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

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

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000002.10:g.71679299C>T

HGVS names

This variant has 26 HGVS names - Show

About this variant

This variant overlaps 17 transcripts.

Variant displays