Original source

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

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

Chromosome 19:5831875 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3896735

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 1 sample genotype.

Variant displays