Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

Chromosome 1:75156982 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000001.9:g.75395255C>T

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays